Zomedica Corp. (ZOMDF) Earnings Call Transcript & Summary
August 28, 2026
Earnings Call Speaker Segments
Operator
operatorWelcome to Zomedica's Fourth Friday at Four Investor Webinar. Today's session is titled Zomedica International, Building a Global Platform for Veterinary Innovation, a focused look at the strategy, the partners and the global opportunity driving the company's next phase of growth. Before we begin, I want to remind current and potential investors that we will be making various remarks about future expectations, plans and prospects that are considered forward-looking statements. There are risks that actual results may differ from these statements. We refer you to the safe harbor statement on screen or to the Risk Factors sections of our public filings which can be found on our website under investor filings, EDGAR and SEDAR +. The statements are made as of today, August 28, 2026, and reflect our expectations as of today. Thank you for joining us for Zomedica's investor webinar series. We're excited to have you with us as we take a closer look at our company. our innovative product platforms and the passionate people driving our success. This series is designed to give you a deeper understanding of how we're delivering value to veterinarians and to our shareholders. At Zomedica, our mission is to deliver innovative diagnostic and therapeutic technologies that empower veterinarians to focus on what they love most, enhancing pet care and improving pet parent satisfaction. Equally important, we help vets with what they need most, streamlining workflow, increasing cash flow and boosting practice profitability. At Zomedica, our mission is guided by what we call our 5 pillars. These are core objectives that shape every decision we make about products and innovation. First and foremost, we aim to improve the quality of care for the pets. Equally important is enhancing the satisfaction of the pet parent, ensuring they feel confident and comfortable with the care provided. Our solutions also focus heavily on improving the veterinarians daily workflow, helping veterinary practices operate smoothly and efficiently. Additionally, we are committed to positively impacting veterinarian cash flow making sure our offerings are financially accessible and beneficial. Finally, our ultimate goal is to increase veterinarian profitability, providing products and solutions that help veterinary clinics grow and thrive financially. Today's session will show how international expansion is not separate from this framework. It is a direct expression of it. Now let's hear from Larry Heaton, Zomedica's Chief Executive Officer.
Larry Heaton
executiveGood afternoon. Welcome to today's Fourth Friday at Four Webinar. I'm Larry Heaton, Chief Executive Officer of Zomedica. Thanks for joining us today. We appreciate you taking the time, and we appreciate your continued interest and support for your company and our progress. Today's session focuses on one of the most important strategic initiatives underway at Zomedica, our international expansion. We've titled this session Zomedica International, building a global platform for veterinary innovation. And I believe the content you'll see today demonstrates why that title was chosen. When we look at the global veterinary market, the opportunity is clear. The same trends driving growth in the United States rising standards of care, increasing investment in diagnostics and therapeutics and growing demand for clinical efficiency are accelerating in markets around the world. Veterinarians in Europe, Asia Pacific, the Middle East and Latin America are looking for the same quality, reliability and innovation that has driven the adoption of our products domestically. Over the past several years, we've invested in the infrastructure and regulatory approval prerequisites to meet that demand. We established distribution partnerships across multiple high-value regions, and have identified additional opportunities in new markets. We secured regulatory approvals that allow us to bring our full product portfolio to international markets, and we've invested in dedicated international leadership to ensure this expansion is executed with the same discipline and focus we apply to everything we do. What makes this story compelling for us as shareholders is the model. We're not building facilities or hiring large international teams. Instead, we are leveraging established credible distribution partners who know their markets and share our commitment to clinical excellence. It's an asset-light approach that allows us to expand our reach while maintaining operating discipline. Today, you'll hear from Paul Tye, our Vice President of International Sales, who is leading the execution of this strategy. You'll hear from Kevin Klass, our Senior Vice President of Sales on how International integrates with our broader commercial organization. And you'll hear from Dr. Rod Richards, who will provide a clinical perspective from outside the United States on how our products are performing in international veterinary practice. Following the discussion of our international business, we'll pivot to a review of our second quarter 2026 performance by our Senior Vice President of Finance and Corporate Controller, Mike Zuehlke. Following that, we'll turn to your questions and comments. With that, let's get started.
Operator
operatorZomedica products are now reaching veterinarians across 6 continents. The company has established distribution coverage throughout the European Union and the United Kingdom for Equine products. with companion animal distribution active in the United Kingdom, Ireland, Italy and Turkey. In Asia Pacific, Zomedica is present in Japan through its own subsidiary and in Taiwan, Hong Kong, South Korea, Singapore, Indonesia, Australia and New Zealand through distribution. In the Middle East, the company is active in the Assisi, including the UAE, Saudi Arabia, Qatar and Egypt. And across the Americas, distribution extends into Canada, Mexico, Costa Rica, Argentina, Brazil, Uruguay and Chile, with additional markets across multiple regions in active negotiation. This is not aspirational. These are established partners, operating through an asset-light model that applies the same platform strategy and cross-sell logic driving domestic momentum. Today, you will hear directly from Paul Tye, vice President of International Sales, on the strategy and partnerships behind this expansion. Kevin Klass, Senior Vice President of Sales, will explain how international fits within the broader commercial organization. And Dr. Rod Richards will offer a clinical perspective on how Zomedica products are performing in veterinary practice outside the United States. Zomedica's international story did not begin with a single announcement. It began with a product that had already earned clinical credibility around the world. It began with Zomedica selling products directly to customers and supporting them from abroad. The company continues that today where an in-country distribution channel is not yet established. PulseVet Shockwave therapy has been used by equine veterinarians across multiple continents for years. Assisi Loop products have also been marketed through international distribution channels in Canada and the Asia Pacific markets. that existing clinical footprint gave Zomedica something most companies entering international markets do not have. an installed base of practitioners who already knew the product and trusted the outcomes. Under current leadership, Zomedica made a deliberate decision to build on that foundation. The company established a structured approach, identify high-value veterinary markets secure distribution partnerships with established credible organizations in those markets and expand the product portfolio available through those partners over time. That installed base did not develop through a single channel. Zomedica's international presence has grown through 2 parallel paths: direct sales to veterinary customers in markets where a formal distribution partner was not yet in place and structured distribution partnerships with established organizations in high-value markets. Today, 29 markets are served through active distribution agreements with an additional 15 markets where Zomedica has placed products through direct sales ahead of a formal distributor relationship. In Europe, distribution covers all major EU equine markets. with companion animal distribution active across key markets like the United Kingdom and Italy and direct sales extending into select markets such as Poland. In Asia Pacific, distribution spans key markets, including Japan, Australia and South Korea, while direct sales have reached additional markets, such as Hong Kong and Taiwan. In the Middle East, the UAE serves as the distribution gateway to the GCC region, with direct sales also active in Israel. Across the Americas, distribution partnerships are active in markets like Canada, Uruguay, Argentina, Brazil and Chile, with direct sales reaching additional markets, including Mexico. And in Africa, direct sales have reached an early market in Zambia. This dual-channel approach is deliberate. Direct sales allows Zomedica to serve demand and build clinical credibility in markets where formal distribution has not yet been established, while distribution partnerships provide the infrastructure for scaled long-term growth. PulseVet Shockwave therapy systems have been sold into 35 countries across 5 continents. Across the Americas, systems are active in key markets, including Canada, Uruguay, Argentina, Colombia, Brazil and Chile. In Europe, placement spans 17 countries, led by markets such as the United Kingdom, Germany and Spain. In the Middle East, systems are in the United Arab Emirates and Israel. And in Asia Pacific, placements cover key markets, including Japan, China and Australia. With additional units tracked across other international markets. This is not a projection. These are active placements with veterinarians who are using the technology in clinical practice today. That global installed base gives Zomedica something most companies entering international markets do not have an existing network of practitioners who already know the product and trust the outcomes. Assisi therapeutic devices have been sold into 32 countries worldwide through a combination of 15 distribution partner markets and 16 direct-to-consumer markets. In the Americas, distribution covers key markets, including Canada and Brazil, with direct-to-consumer sales extending into Mexico. In Europe, distribution is active in markets such as Germany and the United Kingdom. While direct-to-consumer sales extend across additional markets, including France, Italy and Spain. In the Middle East, distribution operates through the UAE. In Asia Pacific, distribution covers key markets, including Japan and Australia, with direct-to-consumer sales reaching additional markets such as China. And in Africa, direct-to-consumer sales have reached an early market in Zambia. The Assisi product line demonstrates the same pattern. Clinical credibility built through direct engagement with veterinarians and pet parents creating a foundation that distribution partnerships formalize and scale. Regulatory milestones have been critical enablers. The CE certification of the Vet Guardian monitor in 2024, combined with existing CE marks across the portfolio, has opened pathways to distribute the full range of Zomedica products throughout Europe, and in other markets that recognize CE certification. International growth at Zomedica is built on a distribution model and the quality of that model depends entirely on the quality of the partners. Zomedica's approach to partner selection is deliberate. The company evaluates potential distribution partners against clear criteria, clinical credibility in their market, established access to the veterinary customer base, regulatory expertise and alignment with Zomedica's standards for training, support and clinical education. These are not transactional relationships. Distribution agreements are structured to support long-term growth. In some markets, agreements are exclusive giving the distribution partner full commitment to invest in building Zomedica's presence. In others, nonexclusive arrangements allow flexibility to serve different segments or product categories through the most capable channel. Today, Zomedica's active distribution coverage spans 4 regions. In Europe, all major EU markets are covered for equine products with companion animal distribution active in the United Kingdom, Ireland, Italy and Turkey. In Asia Pacific, distribution reaches Japan, Taiwan, Hong Kong, Singapore, Indonesia, Australia and New Zealand. The UAE provides Middle East coverage. And in the Americas, Canada, Uruguay, Brazil, Argentina, Costa Rica and Chile are active. The pipeline of additional new markets in negotiation is significant and ranges across Europe, Asia and South America, each representing substantial opportunities. The recent addition of Zomedica's Vice President, International, Paul Tye, provides the resource to accelerate these efforts. A key feature of the model is how distribution agreements evolve. Partners typically begin with 1 or 2 anchor products and then expand to additional product lines as the relationship matures and market traction builds. This land and expand approach reduces upfront risk for both parties while creating a natural pathway to increasing revenue per partner over time. Zomedica also invests in the success of its distribution partners. Training, onboarding and ongoing clinical support are provided to ensure that international veterinarians receive the same level of product knowledge and clinical education that domestic customers experience. regulatory support, including CE marking, import registrations and compliance documentation is managed in coordination with each partner. The international veterinary market represents a substantial and growing opportunity for Zomedica. In Europe alone, the veterinary diagnostics market is estimated at over $4 billion annually with growth rates approaching 10%. The European Equine health care market exceeds $1 billion and is projected to grow at nearly 7% annually through the end of the decade, and these figures represent just 1 region. When you add Asia Pacific, the Middle East Canada and Latin America, the total addressable market outside the United States for Zomedica's product categories is significant. What makes these markets attractive is not just their size, it is their trajectory. Rising veterinary care standards, increasing pet ownership and growing investment in diagnostic and therapeutic technology are driving demand across every region where Zomedica is now active or in negotiation. Zomedica's international revenue performance reflects this opportunity. Today, Zomedica products are sold in 44 international markets across both direct sales and distribution partnerships. International sales grew 18% in fiscal year 2025. In the second quarter of 2026, international sales were up 17% year-over-year. Driven by a combination of organic growth and orders from distribution partners activated earlier that year. Looking at growth drivers. Several factors support continued international momentum. New distribution partnerships are adding geographic coverage, expanding the number of markets where Zomedica products are available. Within existing partnerships, portfolio expansion is increasing the number of products distributed in each market, replicating the land and expand approach we have domestically. Recurring revenue from consumables and assays is flowing through international distribution channels building the same foundation of predictable repeat revenue that anchors the domestic business and regulatory milestones, particularly CE certifications, continue to unlock product availability in European and other markets. International revenue continues to grow. And with a number of markets in active negotiation, we believe the runway ahead remains substantial. The second quarter of 2026 was the best quarter in Zomedica's international sales history. International sales in the quarter reached $1.7 million, that marks 12 consecutive quarters with international sales exceeding $1 million. The TRUFORMA platform delivered the most striking growth with second quarter results up 873% year-over-year. Leading Zomedica's international expansion is Paul Tye, Vice President of International Sales. Paul brings extensive experience in the international veterinary marketplace and is responsible for building and managing the company's global distribution network. Here is Paul on the strategy behind Zomedica's international growth.
Paul Tye
executiveIdentifying and evaluating distributors is done in multiple ways. Of course, I do believe we have a very strong advantage with my 35 years of experience in the industry globally. And my networks contacts and connections I already know many things national distributors worldwide. We're also understanding the from the -- those will be appropriate infrastructure, core products carried, including competitive. Due diligence is important, having a check is to ensure the financial security, track record of growth, market success and obviously having a good reputation within their respective markets. We do an introductory process from an initial meeting to the next phase of signing an NDA, detailed presentation for both Zomedica and a potential partner to understand the cultural fit and competencies. Whilst that's important site visits to inspect the infrastructure confirm capabilities, meet the way employees and also buy 1 or 2 of their key customers is key to making sure that we have the right potential partner. This will build a picture for a long-term partnership and success. A key factor to success for our partners is a very strong and mutual cut relationship. Investing time into that partnership, ongoing and consistent training, regular visits and of course, close support. Now of course, need to be really invested and excited about Zomedica products and dedicated a focused sales team and good internal support across their operations and for infrastructure. And lastly, strong lion market knowledge with an excellent customer base. Interaction, of course, Europe is the big market outside of North America. So therefore, the first target will always be the Nordics, U.K. and Ireland, Germany, France, Italy, Spain and Benelux. We're slightly close behind is Latin America and the Asia Pacific regions, which are exciting, rapidly growing a key market for us to enter. What's really key to understand is that whilst the biggest readers have the largest total potential, this does not always mean that they are the easiest to enter Europe with its multiple countries, cultures, languages, given size complicated markets or also a vice penetrated markets competitively. So it's key for Zomedica for us to use our U.S. -- niche unique products and therefore, limited competition, and therefore, not in the appropriate country market to enter, comes from when the opportunity arises, experience knowledge and who you know. And this is where I believe that my experience in the industry will help us deliver that strategy. Carrying myself commercially and Dr. Richards, our technical expert and vet based in Switzerland, who are part with data are the general contracts and have a close relations with customers. However, we also, of course, leverage the large U.S. operational support teams to offer customer technical support data, training expertise. We also leverage the U.S. via teams and virtual meetings. As we grow and have scale, we will bring in more local support for language, time so coverage and account management. It's important that as we grow and have more international coverage that distributor partners get the day-to-day of support they need to be successful. Over the next 12 to 24 months, we have some key priorities. Of course, one is to support our existing parts add to their portfolio, continue with our support and training and help them grow within their markets. But also to expand geographically internationally and to expand our footprint within multiple countries with new distributor partners. We're working on some existing contractual developments to date, which we are hoping to exploit and to execute over the next few months and continue to expect big priorities, of course, multiple countries within Europe but Asia and Latin America are also high priorities for us to expect.
Operator
operatorPaul and his team are executing a disciplined approach to international expansion. Identifying the right partners in the right markets with the right capabilities to represent Zomedica's portfolio. International distribution at Zomedica does not operate in isolation. It is fully integrated into the company's broader commercial organization under the leadership of Kevin Class, Senior Vice President of Sales. Here's Kevin on how international fits within the overall sales strategy.
Russell Klass
executiveInternational sales is a really important part of our overall sales strategy. We have established products in the United States like PulseVet and TRUFORMA that have high demand outside the United States and going through distribution helps us get better worldwide reach. As we launch new products and learn more about them in the United States, we can leverage these established distribution networks for a more rapid launch. The top products selling outside the United States are Pulse met partly because of the known entity within the equine industry. It is just far and away superior to so much else that's out there. We've gotten tremendous adoption. We also have some great international distribution partners for that product. TRUFORMA is right behind it and the factory pharma right now is probably growing faster than anything else, again, given our ability to leverage the equine business. but also the differential factor that we have in small animal. The 2 hot international products that I mentioned, PulseVet and TRUFORMA, both have very nice recurring revenue. And as such, it helps us grow that business in compound on an annual basis. And as we launch additional tests on the true format, that becomes even more so. We have a few key players within the United States that support both the U.S. and international markets. And these people know a lot about the products and can leverage that experience as we go international and to work with Paul, who's our key person internationally. Additionally, our marketing team has created materials and studies and so forth that can also be leveraged internationally. So we have a head start when we go into a given geography. We do sometimes learn some things internationally that do help us in the United States. Obviously, if we get additional languages, foreign instrument, as an example, we can leverage them in the United States. Also, things like reporting units on the True Pharma, for instance, was the demand that we had outside the United States that may be a preference within the United States. So generally speaking, the earnings are from domestic to international, but it does sometimes look the other way.
Operator
operatorThat organizational alignment is critical. It ensures that international growth is supported by the same commercial infrastructure, product expertise and clinical resources that drive domestic performance. The strongest validation of any international strategy comes from the clinicians using the products. Dr. Rod Richards is a veterinarian with experience practicing outside the United States with direct experience using Zomedica products, particularly PulseVet Shockwave therapy in international clinical settings. Here's Dr. Richard on what he has observed.
Roderick Richards
executiveHello Dr. Rod Richards with Zomedica here. I started shockwaving with the Equitron in Singapore in the late '90s and found the results so amazing. I joined the manufacturer in Switzerland. I've been managing the international business for the company, PulseVet and been with Zomedica for 7 years now. What I've observed is that the international performance source community is extremely well connected, which means that new products coming onto the market, which really improve the management of Equine athletes gain acceptance and uptake around the world. This is why the PulseVet system is still so very popular globally. Pulse is clinically effective and Equine vets around the globe understand the benefit that Pulse can bring to their Equine patients. PulseVet is a unique product. It is the smallest electrohydraulic shock wave system designed for use by veterinarians in practice or on the road. The electrohydraulic technology brings clinical advantages, which means shorter and fewer treatments than other devices can achieve. In addition, there are numerous scientific studies using PulseVet, which showed clinical efficacy. In a word, PulseVet is incomparable. TRUFORMA is a game changer in equine Medicine. Until Zomedica developed the eACTH assay on True former all reference labs had measured eACTH with a significant cross reaction with a peptide called corticotropin intermediate low peptide or pipe. This was and is due to the technology behind the chemiluminescent assays that reference labs use. CLIP does not appear to have a hormone role at this stage. But by measuring CLIP and eACTH together, the true level of eACTH remained uncertain. The bulk acoustic wave technology of TRUFORMA enables vets to measure the absolute value of eACTH in equines for the first time. This is having a major impact on how vets manage wares with PPID today and going forward. In a word, TRUFORMA is incomparable. Horses generally respond very well to shockwave therapy with pulsed and with 0 significant side effects. This gives our customers confidence to treat and experiment a little, thanks to the pioneering work of one customer, we've been developing therapy for asthma and EIPH and horses which is showing good results. Who would have thought such a therapy would be a reality, and there are more conditions being investigated at this time. Geriatric dogs can also benefit greatly from therapy with PulseVet. I have seen the comfort it can bring to owners who have an old dog with, for example, chronic back pain and intolerance to assay therapy who responds well to PulseVet. The accuracy and dynamic range of TRUFORMA gives veterinarians unique assays and also reference laboratory precision in the practice. This will improve the medical care of our companion animals and horses greatly.
Operator
operatorClinical validation from practitioners outside the United States reinforces a key point for shareholders. Zomedica products are not simply being exported. They are being adopted, integrated into international workflows and delivering outcomes that meet or exceed the standards veterinarians in those markets demand. Zomedica's international product ecosystem follows the same logic as the domestic portfolio, diagnostics, therapeutics and monitoring, designed to work together within the clinical workflow. What differs internationally is the sequencing of how products enter each market. Therapeutics lead internationally. PulseVet shockwave therapy has the strongest global presence with an established clinical reputation in Equine markets and growing adoption for companion animal applications. The Assisi Loop and EquaLoop therapeutic devices established in the Asia Pacific markets are expanding into European markets and Vetagel Hemostatic Jaw, a low-priced universally needed consumable is increasingly being positioned as an entry product for new international markets. opening distribution relationships that create a pathway to larger product placements over time. On the diagnostics side, the TRUFORMA platform has launched in Europe for Equine applications with companion animal potential across multiple regions. TRUVIEW digital cytology is expanding its international availability in monitoring, the Vet Guardian Plus monitor is CE certified for European markets and is being distributed across the United Kingdom, Europe and additional territories. For shareholders, the important point is how these products work together internationally, just as they do domestically, the land and expand model applies. A distribution partner begins with an anchor product, builds clinical traction and customer relationships and then adds additional products from the Zomedica portfolio. Each product added increases revenue per partner, consumables and assays generate recurring revenue that builds predictability over time. and regulatory milestones, particularly CE certifications, unlock the ability to expand the product portfolio with an existing geographic coverage without requiring new distribution agreements. The result is a compounding growth model, more markets, more products per market, more recurring revenue per product, applied through an asset-light distribution infrastructure that maintains operating discipline.
Larry Heaton
executiveThank you. I hope today's session has given you a clear picture of what we're building internationally and why we believe this represents one of the most significant growth opportunities in front of Zomedica. Let me leave you with a couple of key points. First, international expansion is not an experiment for us. It is a deliberate, structured strategy that we've been executing methodically, identifying high-value markets, securing the right distribution partners and building the infrastructure to support long-term growth. Second, the model works. We are reaching veterinarians across 6 continents through an asset-light distribution approach that allows us to grow our international presence without the capital intensity of building operations in every market that we enter. Third, we're applying the same platform strategy internationally that has driven our domestic momentum, the same products, the same cross-sell approach guided by our 5 pillars, the same focus on recurring revenue through consumables and assays. What has worked in the United States is now working across Europe, Asia Pacific, the Middle East and the Americas. And lastly, the runway ahead is substantial. With active distribution across more than a dozen countries and a significant number of additional markets in negotiation, we're still in the early stages of what this can become. We believe international markets represent one of Zomedica's most compelling growth opportunities built on proven products, strong partnerships and a disciplined strategy for global expansion. Thank you for joining us today. We appreciate your time and your interest and support of Zomedica. With that, I'm going to hand things over to our Senior Vice President of Finance and Corporate Controller, Mike Zuehlke, who will walk you through our financial results for the second quarter of 2026, and outlook in more detail.
Mike Zuehlke
executiveGood afternoon. I'd like to begin by wishing everyone an enjoyable fall season as we transition to cooler temperatures and adjust to the return to school schedules. Most importantly, we want to acknowledge and thank you for your continued interest and support of Zomedica as is becoming a trend. I'm excited today to detail another record quarter for Zomedica and continued progress towards cash flow breakeven and get profitability. Zomedica delivered another impressive performance in the second quarter, with revenue increasing and operating expenses and cash burn continuing to decrease. The second quarter of 2026 marked our 22nd consecutive quarter of record year-on-year revenue. Our 37% year-over-year revenue growth was driven by several key factors. First, we continue to see strong demand for our PulseVet and Assisi therapeutic device products. Second, we saw continued adoption of our diagnostic offerings, particularly our TRUFORMA platform. This growth has been supported by collaboration with our distributors including our relationships with Boehringer Ingelheim Animal Health in the U.S. and Canada as well as our expansion into additional international territories. And third, our Development Services segment continued to contribute meaningfully generating another $1.4 million in revenue during the second quarter. From an operational perspective, we continue to execute with discipline. Gross margins remained healthy at 64%. Operating expenses were down $2.6 million or 20% and compared to the prior year. Notably, expenses were down in all 3 report groupings: G&A, R&D and selling and marketing. Our adjusted non-GAAP EBITDA loss improved to $2.3 million compared to a loss of $5.5 million in the second quarter of 2025, an improvement of 59% for the first half of 2026, our adjusted non-GAAP EBITDA loss has improved 58% versus the first half of 2025. Finally, cash burn improved by $2.1 million, representing a 38% reduction in -- from the second quarter of 2025. Looking ahead, our priorities remain clear. accelerating global adoption across our innovative portfolio, expanding our recurring revenue streams via our consumables products and continued progression toward an achievement of cash flow breakeven and profitability. We believe our record second quarter performance, expanding commercial partnerships, ongoing activity within our Development Services segment and strong balance sheet all position us well for the remainder of 2026 and beyond. We remain focused on executing our growth strategy, improving operating efficiency and creating long-term shareholder value. I will now provide more detail on the components of our strong performance, beginning with revenue. Total revenue for the second quarter was $9.5 million, an increase of 37% compared to prior year and a record for the second quarter of the year. The 37% increase over the prior year was highlighted by the following: our core products, which encompass our diagnostics and therapeutic devices segments were up 16% compared to the prior year, representing the strongest second quarter in the company's history for our core product portfolio and demonstrating healthy organic demand across our business. Diagnostics segment revenue increased 77% for the quarter and is up 75% year-to-date. As a result of continued adoption of our TRUFORMA point-of-care diagnostic platform and the utilization of our expanded menu of assays, notably among equine veterinarians. Therapeutic Devices segment revenue increased 9% for the quarter, driven by the continued strength of our PulseVet and Assisi products. Capital revenues, which we have stated before, can be choppy, increased 14% over the prior year. which we anticipate will drive consumables revenue growth in future quarters. Our Development Services segment contributed another $1.4 million during the second quarter, bringing the year-to-date total to $3.4 million and $6.4 million in total since we introduced the segment in the second half of 2025. Across all segments, our consumables revenue increased 26% for the quarter and is up 24% year-to-date. This growth is again driven by continued demand for our TRUFORMA of products as well as sustained demand for our pulse patrols, which comes from both new device installations and reorders associated with existing systems. We expect consumables growth to further compound as our installed base expands. Our international business also continues to perform exceptionally well, with revenue increasing 17% in the second quarter driven primarily by organic demand. And we anticipate that our expanding global business will continue to contribute meaningfully to the sustainable long-term growth of Zomedica. We remain committed to the pursuit of strategic opportunities that leverage our existing asset base and scale to drive incremental value for our shareholders within both the human and animal health sectors. Moving to operating expenses. Total operating expenses for the second quarter of 2026, were $10.1 million, a 20% reduction when compared to prior year. For the year, we are down $5.3 million or 21% after adjusting for a noncash impairment charge taken in the first quarter of 2025. Operating expenses as a percentage of sales improved 75% for the quarter and have improved 79% year-to-date. Reflecting our commitment to disciplined cost management and the realization of scale in which the company has invested. We anticipate continued operating leverage as sales continue to grow across all segments and this growth is supported by our current cost structure. Research and development expenses were down $0.8 million or 43% for the quarter and are down $1.5 million or 41% year-to-date. While spending is down year-to-date primarily as a result of recent product launches, we anticipate that our R&D spend will moderately increase as we continue to develop next-generation offerings and pursue solutions to unmet or underserved market needs. Selling and marketing expenses were down $1 million or 21% for the quarter and $2.2 million or 22% year-to-date while revenue has increased 37% for the quarter and 36% year-to-date. General and administrative expenses were down $0.8 million or 13% for the quarter, bringing savings to $1.6 million or 13% year-to-date when compared to prior year. This continues to reflect disciplined cost management and efficiency gains. Turning to the balance sheet. Zomedica ended the quarter with $44.1 million in cash, cash equivalents and available for sale securities. Cash used during the second quarter was approximately $3.4 million, representing a 38% reduction compared to the cash burn in the second quarter of 2025. This represents our lowest non year-end quarterly cash burn on record since commercialization. Year-to-date cash burn has improved by $3.2 million, reflecting continued fiscal discipline, while supporting top line revenue growth. As always, I would like to remind you, we remain essentially debt-free. Continued top line growth at healthy margins, combined with the operating discipline that has resulted in reduced operating expenses continue to move us towards our goal of cash flow breakeven and GAAP profitability. As evidenced by both the reduced second quarter cash burn and a 59% reduction in our adjusted non-GAAP EBITDA loss. Our results for the quarter continue to illustrate that your company is in strong financial health and making meaningful progress towards cash generation and profitability. Importantly, we believe we are achieving these results while remaining well positioned to fund and support our ambitious growth strategy. I would like to close again by expressing our gratitude for your continued support of and interest in Zomedica. It is an exciting time for the company, and each earnings release provides further evidence of our progress and our commitment to creating and delivering long-term shareholder value. With that, I'd like to give the floor to our CEO, Larry Heaton. Larry?
Larry Heaton
executive[Operator Instructions]. Okay. So again, thanks, everyone, for joining us and for your support of Zomedica. I will dive right into the Q&A. And this week, I remember that we asked when you signed in or when you register, if you had any questions for us, and so I'll make sure and grab those as well as the ones that you're entering now into the Q&A section. All right. So the first one. I noticed that you have issued social media mentioning the shortage in eACTH testing at reference labs is there an opportunity here for Zomedica. So a really good question. And this is information that is public because it was made public by the reference labs themselves. And people know this, how material that will be, I guess, we'll have to sort that out. the major reference lab that offers eACTH testing in the United States is a university hospital in New York. And earlier this month, they sent a letter out to all their customers that indicated that due to a back order of the reagents necessary to run the test for eACTH on their ammulite machine that they were not going to be able to run any tests after around the eighth of August, somewhere in there. Maybe it was the fifth or whenever it was and would not be able to begin redoing the test until the reagents were off back order, which they indicated would be in early mid-October. Incidentally, all other reference labs, there's one other university and there's a couple of large companies you've heard of, offer this test somewhat, not the prevalent providers, but they also use the ammulite machine and are also subject to the same backorder. For that matter, we use the ammulite machine in our own R&D. And if we needed that, we'd be a back order, too. But we don't need it. It's not needed for the TRUFORMA device. We use the BAW sensor, as you well know. And as a result, TRUFORMA is not affected by that back order. So when we heard this, we were concerned that our veterinarians out in the United States and Canada would be disadvantaged by not being able to get that eACTH test to run at those reference labs. And so we've reached out. And so has BI Borne Ingelheim in the United States. And so has Bohringer in Canada have reached out to let -- and we've done it through social media. We've done it through e-mails with customers. BI is doing it through their sales force. We're doing it through our sales force. And since this is actually a very prime season for testing horses for -- with eACTH for PPID. It's been a really busy days of August. We have been very busy placing new TRUFORMA of devices in equine practices, both in the United States and Canada. Both from our own efforts and also in collaboration with Borinkheim. It's certainly the case that some of these customers may choose after these research lab or the reference lab is able to come back and start doing them again. Some of the customers might go back to them, you can be sure that we're doing every single thing we can to equip them to be able to do the testing themselves and experience the benefits of having results right there within 15 to 20 minutes as opposed to having to send to a reference lab after first taking the sample, chilling the sample until they get it back to their clinic, freezing the sample, setting a frozen to the reference lab and then waiting for the results. So yes, there is an opportunity there for us, and we are basically all over it. All right. Next one, still on assay. Should we expect to see more than 4 assays. Let me read it exactly. Now that Zomedica is approaching profitability in the TRUFORMA installed base continues to grow. Does the company's strategy for new assay launches need to evolve as well? Should investors expect to see more than the current pace of roughly 4 new assays per year with new assays potentially being introduced throughout the year rather than concentrated toward the end of the year. So it's a good question. I think for 2026 -- well, this year is almost over, right? And for 2027, you should expect essentially the same pace in terms of the rollout of new assays. And this is because we're trying to balance R&D spending with a new assay development. As you heard a little bit earlier from Mike, R&D spending is down about 43%, I think you said, year-over-year. And some of that -- not all the R&D spending goes to TRUFORMA. So as you know, we recently launched the acoustic Muffler and things like that. So we, as you know, are striving to reach cash flow breakeven as soon as we can, targeting fourth quarter of this year and certainly for 2028 -- 2027. We expect for the full year to be profitable. And so we're going to keep that spend down a little bit. I know there's a trade-off, but I think our shareholders are best served by us maintaining that reduced operating expenses and get it to cash flow breakeven as soon as we can. We do have a number of assays that we are rolling out yet this year and into next year. As far as the pacing, it takes about a year to develop an asset. There's kind of a lot to it. I think we -- if you're curious, we have the webinar on TRUFORMA, and I think they go through all the different phases, it takes about a year. And so it's going to take some time to change that cadence. What we'd have to do is start new assay development in different quarters. Certainly, we can do that. We have not done that this year for reasons that we just talked about. But we'll likely get to that in 2027. We'll maybe start in the second quarter, third quarter, fourth quarter, things like that. So that's that.
Unknown Executive
executiveLarry, I think it's also worth noting that the pace of 4 assays per year is significantly better than most -- I think anybody else in the marketplace. I mean it's -- there are just not assays popping up on a regular basis from anybody else.
Larry Heaton
executiveYes, a good point. We're not anybody else though. So we'll definitely do what we can there, right? Next question, has Zomedica Explore developing assays for diseases found in cattle livestock, for which there are no pen side or point-of-care testing available? If so, would FDA requirements govern approval? The FDA requirements would not kick in for assays for the kinds of things that we're testing. We're testing for if you were going to produce drugs or vaccines or something that would go in account, then actually, it would be the FDA or the U.S. Department of Agriculture that would get involved. But it wouldn't be a factor for us. What's more of a factor. I mean, we'd actually love to do that, right? There's a lot of cows out there and so on. The thing is, it's not like when your dog gets sick or your cat gets sick, if a cow gets sick, it's not necessarily going to be diagnosed and treated and brought back to health. There may be some like really expensive cows and things like that, and those will find their way to an equal invent or a large animal vet and then there, we would be in that practice if we have something applicable to them. The other thing there is that single animal testing because it's -- they're not looking to see a cow with signs or symptoms and then test what's going on with it. They move it away and so on. And so the incidence of testing a single animal is not great. if they're going to test all the cows, all the herd, the whole herd, then our systems just -- it's not set up for that. The throughput is just not -- it's not fast enough, right? If it takes 15 minutes depending upon the assay to run a test, and you have a herd of 500 cows. They're going to -- they're probably going to look for some other way of doing it. Having said that, pretty much every strategic review we do, we ask ourselves, isn't there something we can do for the cows and sheep and goats and everything else. And so far, the answer has been not just yet. Let's see. As Zomedica expands internationally, can you provide some measurable targets for investors such as the number of countries, distributors or international accounts you expect to have over the next 12 to 24 months? And when you expect international sales to become a meaningful percentage of total revenue. Kevin, do you want to take that one?
Russell Klass
executiveSure. Be happy to. First, I'd argue that our international sales are already a significant percentage of our revenue at about 20%. And they are growing at a rate that's a little faster than our domestic rates. So they are becoming more and more significant every year. With respect to new distribution, I mean, Paul has been on board for 6 months and the number of distribution opportunities he's identified is amazing. But you also heard him talk about the process of bringing in distributor on board. There are several steps to it takes a while. Also, it's not just bringing on a new distributor. Sometimes it's expanding our products within a distributor. So adding TRUFORMA to a distributor. But then after that, it's adding additional assays to the analyzer that's already at a distributor. So there's multiple ways that we can grow internationally. I don't know that I have a number of distributors that we're going to add in the next year, but I can tell you that we anticipate a very significant international growth and for that to be even more a percentage of our total sales than it is today.
Larry Heaton
executiveThank you Can you discuss the muffler? Is this on the trot itself? So when you order a new trail, you get one? Or is it an additional order on top of the trode? Can this be material or just an additive feature to help sales? I think the quick answer is it's an additive feature. It's literally an accessory that's used in conjunction with the trade we will -- we are and will include this acoustic muffler with each new post that system that we sell. One for a small animal practice that uses the extra and actually 3 for the 4 trodes that are purchased by equine vets. It is something that doesn't permanently attach to the device, it snaps on it. It's used and then it snaps of so the trade and the muffler itself can be cleaned. While we are going to provide them along with the instrument, remember, we sell the system for -- I think it's around close to 35,000 when you add the rode to it for small animal and close to 40,000 when you add the 4 drones for equine. So we're going to provide them with an acoustic buffer at no charge. We will sell them, and we have sold some where people just didn't want to wait for the rep to get to or whatever, so it was $125. But that's not going to move the needle. In terms of a materiality standpoint, unless Mike corrects me on that, but I don't think you will. But what it does do is you put this muffler. This acoustic muffler on the trade, and it reduces the noise to sound by 75% to 84%, depending upon which tone you're putting it on. And that is that's a pretty significant change. Not so much for equine bets that are doing these treatments out in the yard or the barn or something like that. But when you get into a small animal practice, it's loud -- and so it's not painful, it's not harmful, but it's still low. And so actually think it's not bad because it everybody in the clinic, here's the click on the pulse that and on, hey, what's that? Does my dog need that. But in any event, it's a good thing, and it will help us to push off any competitor that says, look, our thing is quiet. I mean our standard response has been, it's a sound wave, it should make noise. And that's -- you get the effectiveness with the noise. So anyway, so that's that. Let me go to some of the ones from the -- from the registration list. TRUFORMA assays are not mentioned enough, bring out details. So I'm not sure who that person is, but we can talk a lot about this and have, and we'll be happy to. But we're not going to list out -- we're not going to give details of which assays we're rolling out. And I've covered this before. It's a competitive issue. I mean, just this month, IDEXX proudly announced to the whole world that they had just introduced a new assay for Animal Health at the point of care that was the first time it was available to point of care. We've had it on the market for over a year. So we don't want to give them any more of a head start for that. And it wasn't one of our top-performing assays. So I don't worry about what it's going to do to our TRUFORMA business, we're going to be just fine there. But I'm going to be a little scarce on details for that. Let's see. What milestones must be achieved to be relisted and what does the time line look like? Can you narrow down profitability date? So I think there's 3 sort of levels of milestones. There are some that are company determined. There are some that are exchange determined and then there are some that are market determined, right? So if you look at the company determination, we're not going to seek relisting until we are cash flow positive and profitable. and narrowing down the profitability date, as I've said before, we expect to be profitable for the full year in 2027. And so -- and that's -- I think someone else asked a question here. Does that mean GAAP, adjusted EBITDA, cash flow, it means all those things for 2027? As I mentioned before, we're shooting really hard at getting to cash flow breakeven in the fourth quarter just a function of continuing to increase revenue, keep expenses down and execute financial discipline. But beyond that, what are those determinations, right? So one, we want to be cash flow positive and get profitable. With respect to the exchange, they have all sorts of criteria. Mike has gone through these before. It has to do with your capitalization and the number of shareholders and whether you're audited and so on and so forth. We meet all of those requirements for pretty much all of the exchanges that we've encountered. The one that we don't meet for any of the exchanges currently is the share price. And so that brings us to the market-determined factor, right? If the share price rises to the point where we're eligible for joining an exchange, we'll do it ASAP. In order to get there, we need given that we're not inclined to do some sort of a capitalization structure adjustment, I think you all know what I'm talking about. Given that, that we're not inclined to do that. Then once we get to cash flow breakeven and profitable, we can consider a share buyback to reduce the float. And beyond that, it's a matter of patients continuing to drive good results and so on and so forth. So we'd love to be on a different exchange and we'll work hard to get to that point. What does the future share price look like? Well, if I could answer that, I think I'd be trading stock somewhere, right? As a shareholder, I hope it's higher. As an analyst, someone that analyzes all the metrics and facts and figures, I calculate, in my opinion, in my calculation, that it should be higher. But as a member of the management team, I'm just going to work my ass off to get it to be higher. And I think that reflects the sentiment of all of us here at Zomedica and all of us, our shareholders right alongside with those of you on this call. Let's see, that might be all the ones from there yes, here's one, Secura partner-funded human bulk acoustic wave deal, upfront fees, milestones, royalties and Zomedica manufacturing without dilution. So I'm not sure that, that's a question, I guess. It's a good idea for sure. It's one that you may have noticed that we were actively pursuing as evidenced by our financials where we're generating revenue from that. And we will certainly keep you up to speed on all of those things. Okay. How is the Q3 earnings report shaping up? Mike, do you want to take that one?
Mike Zuehlke
executiveSo Larry discussed a little bit about the opportunity that came our way with the emulate back order situation. what I would advise is or we don't provide precise guidance on the numbers. I would tell you that all the metrics that we've come on each quarter for the last several quarters since I've been the voice on these calls expressing year-over-year record revenue, declining OpEx, declining cash burn, we're all on track to continue the trend of those metrics in the third quarter of 2026.
Larry Heaton
executiveYes. That's a good answer. Let's see here. Any updates on the future human health collaborations? We will update you just as the developments occur. I think you've all seen some of the -- or maybe some of you have seen some of the recent knowledge that's information that's been shared by Ram with the cell guardian. It's had a pretty impactful pretty significant impact on patients and as they continue to evolve, we're their partner there. And we continue to work with other human health partners. And just as soon as we have something that's definitive. When you work with the human health partner, there are phases and waves of work you first are exploring whether or not there's there. And then as you figure it out and you say, yes, there is the then you make a plan to start developing. And then if it shakes out a certain kind of way, then you're doing other things and it grows and builds over time, and it's a little wavy. We've signal ourselves. You've seen that in the revenue. And so for us, we will not name partners that we're working with until we execute an agreement that is defined. And has what has enough information and it is for you to assess what the impact on the company may be as we move forward. What does full year profitability? I mean, I think I've already answered that one. The stock has very little volume. How can we get more investors interested. I would welcome all of your suggestions in that area -- made a conscious decision not to sort of -- our experience has been that the institutional investors are going to wait until the share price is higher or until we're on a different exchange or until we have a significantly reduced flow. So and while there's not necessarily an expensive presenting at those things, there is an expense in traveling and time spent there instead of doing something else. So talk to your friends, talk it up, I certainly do. And I think it's not going to help with volume so much, but with price. I mean, no one's buying my shares and the management team here, we're not looking to sell shares. And so even if there's low volume, that doesn't necessarily mean the price can't appreciate if people are stingy with their shares. But that's an individual decision that every single shareholder has to make, and I certainly recognize there are times when you have to have -- you have to trade cash for your shares. So it makes perfect sense. There's a question here about a tiny acquisition, and I'm not sure what it means, so I'm not even going to skip it because I don't know what I would be answering. Which cattle biomarkers could meet our pricing and volume requirements and would any require? I think I've already talked about that. I don't really think there's an opportunity for us there in the near term. When will BI launch in Europe? And what is the holdup? Do you think this happens by year-end? I will let BI make their own determination and their own time frame. We not so long ago, got TRUFORMA into Europe. In Canada, we have been selling TRUFORMA individually to accounts for a while, handling them direct. But we've recently engaged a what's called a 3PL or a third-party logistics provider so that it avoids and eliminates any customs issues. We have TRUFORMA. I think we got it in to grow that last year, so it's European-wide. But there needs to be a critical mass of the ability on our part to provide the instruments and so on and so forth. Also, the way that they get their test done can vary a little bit. So I will leave that up to BI EU. So far, the success of the venture in the United States from their perspective, led to their BI Canada unit, embracing it and they've gotten off to a really, really good start. Now, of course, it's also propelled by the fact that their other partner this reference lab in New York can't do the test. So I noticed no insider buy since Q2 earnings was released, any reason behind us. Yes, there is a reason. I'm advised by my General Counsel at my best approach for this kind of question is to not answer it and not comment on it, but I will tell you that -- as you know, there are things that if we're aware of things that are coming down the pike, that would give us an unfair advantage in terms of buying the shares that we can't buy the shares. We adhere to that policy. I certainly would like to buy some more at $0.08. What is the 2027 international revenue target? And how many distributor agreements are currently in final negotiation? I think we've answered that question. We're going to get to cash flow breakeven and profitable in '27 in our belief at this point. and the rest of that would be information that we're going to kind of hold to ourselves. Do you think the insider window will be opened in November after you report? Let me answer that question in November. Has the Muffler approved small animal pulse hit sales conversions or treatment utilization and how will Zomedica measure that? I don't think it's going to affect utilization at all. If you have a customer that's been used in the pulse bet on small animals, and they see that dog walk out of the exam room when they had to live in or be carried it. they don't care about the noise. It's not egregious. But if you're considering buying a device and then there's a competitor out there that has a really quiet one, then you might not -- you might take a pause and try theirs out, we have plenty of data that show that would be -- from a clinical standpoint, that would be an ill-advised move but not -- but having that and the muffler certainly enhances our opportunity to go ahead and get that sale quicker than waiting PIM status. Actually had a print on that. We're on track to do that. We have clinics that are currently using with the -- I think we're up to around the 3 top PIMS providers are currently using in an author beta test or whatever, but everything is going smoothly. And we're about the business of bringing in all the other devices that we have to that PIMS capability. And as we said, we expect to have that out into the marketplace by the end of September. And yes, so we're on track for that. And I think that will be meaningful in the small animal market, somewhat in the equine market as well. But for sure, in the small animal market. does current development services revenue include a human BAW program and any milestone or royalty agreement signed. If we had agreements signed, we would have disclosed them if they were material. We have disclosed material agreements before. And in fact, we've disclosed the agreement for even though it might not have been certainly in the early days of material. Does current development services revenue today include a human BAW program? Yes. How many human health programs are currently paid and what percentage of development services revenue comes from Ram? This is not a breakdown that I'm going to provide is out of courtesy, both to Ram and to our other partners. If we become breakeven by Q4 of 2026, could you possibly start buying shares back at the end of 2026? Getting the cash flow breakeven is the first and the most immediate milestone we expect to achieve getting to positive EBITDA and getting to GAAP profitable are the more -- are equally important. Some people may believe they are more important. So I'll leave that for people to decide for themselves. But we'll get there before we would entertain the idea of doing a buyback. And realistically, there's a lot of shares out there. And we have to balance -- we've said it before, right? A buyback is a permanent loss of capital for a short-term impact on the share price. What's obviously more impactful on the share price over time is that we introduce a new product or introduce a new initiative or something like that. So we'll have to carefully balance that. And there are a lot of innovative ways to look at how you might address the capital structure in conjunction with the share buyback. But those are things for another day. And frankly, another year, it won't be in 2026. Publish quarterly KPIs, installed system, cartridge utilization international revenue and the development services backlog? Yes, our competitors would be thrilled by that. And so I'll say for the uptime time that we don't have any intention of doing that. We allocate our revenue and so on through our segment reporting, which we believe is we believe is sufficient. Let's see, which 3 PIMS platforms are in-clinic testing, how many clinics are participating and win is full commercial launch? Well, I just mentioned commercial launches end of September and into October, November, the 3 platforms, one off the top of my head is EasyVet. I don't have the most recent list in front of me, but they are the next 2. If you Google what are the most popular PIMS programs in the U.S., the top 3 would be the ones that we're involved with right now. But it really doesn't matter because our intention is to get to essentially all of them by the end of next month. We're working with an integrator, right? So what that means is that there's us, our MisoMedica platform, and then there's an integrator third party that we're working with. And then there's all these other systems. The integrator already connects to all those other systems for other companies and other products. So there's no new thing there for them. We just have to connect a particular device. And then what's involved in validating it is put it in a clinic and make sure it's working without any bugs. And so there is that. Let's see. I think we're getting to the end here. Is the page human BAW program separate from Ram and could it lead to recurring commercial manufacturing revenue? Yes to both, separate for Ram and it could lead to that. And okay. So we're now about 11 minutes past. I think I've gotten to pretty much all the questions. There are some more that I know if I was an analyst and creating a model, I'd love to have answered, but we're being a little close to the vest because we think that's in the best interest of the company and by reflection of shareholders. So with that, Paul, any other comments?
Paul Tye
executiveNo, I think has been going extremely well. I think overall, I think we've detailed out the excitement we have about the international expansion. And I think what's important to say is that as we look at the number of opportunities that are coming towards us, some are regions that we're looking at, which have multiple countries. And I think that will expand very quickly, and we'll see the fruits of that over the next year, 18 months. So it's very exciting times.
Larry Heaton
executiveYes. So I'm happy you're here, but yes, because you've really picked it up and accelerated it and I think that's great. Kevin, any other comments?
Russell Klass
executiveNot only just -- I'm also very grateful to have Paul here. And I think we will be accelerating our international growth at a much faster pace than we may have otherwise been able to. So all keep it up.
Larry Heaton
executiveAnd Mike, how about you?
Mike Zuehlke
executiveJust quickly on the comment about the KPIs. What I would add to your answer, Larry, is -- our reporting regulations require us to disclose financial performance at the level at which we run the business at. So while, again, I echo Larry sentiment so why those KPIs would be valuable to analysts and also competitors. And we're certainly not blind to what those KPIs are, but the total addressable market out there for us is so significant that opportunities aren't what we lack and it's full steam ahead. cash flow generation, profitability and then growth beyond that, right? So I get equally excited every quarter when we have great results to report, and I look forward to doing so again at the end of November.
Larry Heaton
executiveThank you, Mike, Kevin and Paul, and thank all of those in attendance for your continued support of Zomedica. I will tell you that we are committed here to continuing the track that we're on, increasing revenue providing really good margins, decreasing expenses, not just as a percentage of revenue, but also in real dollar terms. And all of this is for one reason and that is to build the value of your company. to increase the value that you have as shareholders and what you hold in Zomedica. What we all hold into Medica. And with that, thank you again for fourth Friday. Next, Fourth Friday, we'll be focused on the marketing efforts at Zomedica. And it will be -- well, Fourth Friday in September, I think that's whatever it is. All right. With that, all of you have a great weekend and take care.
Read the full transcript via the API
You're viewing the first half of this call. Get the complete Zomedica Corp. transcript — plus 253,000+ transcripts from 12,000+ companies, speaker segments, AI summaries and full-text search — through the EarningsCalls.dev API.
Get the API View API docs →This call discussed
For developers and AI pipelines
Programmatic access to Zomedica Corp. earnings transcripts and 253,000+ others is available through the
EarningsCalls.dev REST API. Plans from $24.99/month — full transcripts, speaker segments,
full-text search, and the recently-added /api/v1/transcripts/recent polling endpoint for ETL pipelines.