James Green
Analyst · Benchmark
Thank you, David. Hello, everybody. Let's start by moving to Slide 3 of the presentation and take a look at the highlights for the quarter. First, I'll say that I'm pleased to see strong growth in North America. However, similar to numerous life cycle tools companies, we did see -- we were impacted by post COVID, lower demand in China and Asia Pacific. Going to the numbers; revenue for the quarter was $25.4 million. That's down 6% from last year on an as-reported basis. This revenue includes a net effect of $1.3 million of discontinued products compared to the prior year period. Q3 revenue saw a net positive FX effect of $700,000. Adjusting for both FX and discontinued products, our underlying core revenue was down roughly 3.5%. Gross margin improved to $14.7 million or 58% of revenue, up from 45% in the same period of FY '22. However, this prior period included inventory write-down that impacted FY '22 comparable by about 5%. Adjusted operating profit improved $1.8 million or 7.3% of revenue, up from $700,000 last year, an improvement of $1.1 million or nearly 5 percentage points. Adjusted EBITDA measured $2.2 million or 8.9% of revenue, also up 5 percentage points from the prior year. GAAP earnings per share was $0.03 loss, an improvement from an $0.08 loss last year. Adjusted EPS measured a positive $0.01 per share, up from a $0.01 loss last year. Cash flow from operations was $4.4 million versus $600,000 last year. In the appendix, you'll find the bridge from GAAP measurements to adjusted or non-GAAP measurements. Now let's move to the next slide, Slide 4, I look at the revenue by quarter by product family and with an improved regional view. Starting with the Americas. Revenue was up 5.9% as reported and included 5.2% of net reduction of discontinued products. So considering discontinued, our underlying core revenue grew by about 11%. Pre-clinical had strong growth in our core tech telemetry and Penema enterprise software though somewhat held back by post-COVID lower needs for respiratory products. Cellular molecular products were down primarily on discontinued low-margin products and some slowness in cell-based testing systems. Moving to EMEA. Overall, EMEA revenue was down 1.4% as reported and included a 6.2% net reduction from discontinued products but also had a positive FX impact of 7.7%. Adjusting for FX and discontinued, EMEA was down roughly 3.5%. Now moving to China and Asia Pacific. Q3 reported revenue was down 30%. And FX and discontinued products had a modest negative effect of approximately 4.5%. The primary impacts were twofold. Preclinical saw a big drop in demand in preclinical respiratory products where during the COVID years, including 2022, China had significantly purchased for COVID research. However, our core telemetry and Pania enterprise software closed close to flat. CMT saw a measurable drop in cellular molecular products where, again, during COVID, China had strong demand in academic research. We move to Slide 5 of the presentation. I would tell you a little bit about some of our exciting new products and new introductions that we'll be showing and showcasing this next week at the Society for Neurology Conference. As you know, over the last 3 years, we've optimized our product offerings to target key technologies in the drug and therapy development continuum. Our product strategy is to continue to introduce new technologies and applications in leading academic research labs and pharma discovery, while at the same time, adapting these technologies to further penetrate larger industrial applications with our customers in pharma and CROs and biotech. Following the strategy, next, we will be showcasing a number of these offerings and I'll talk a little bit to you about 3 in particular here. First, we'll be highlighting our new mesh microelectrode-eray platform. these new mess MEAs are targeted for use in organoids, which are small tissue segments or cultures that we believe can represent a proxy for many organs such as brain and heart. Organized are a promising growth area for academic research and discovery as well as safety pharmacology and toxicology. Our new mesh MEAs build on our recognized leadership position in single well high-density micro electrode arrays used heavily today, enabling precise signal measurement from within the organoid. We're excited to be presenting early research results using this novel technology on brain organoids at next week's Society for Neurology. Next, we'll highlight our new VivaMARS high-capacity behavior monitoring systems. We first announced our initial customer order last April. The VivaMARS system is specifically adapted to high-volume multi-animal model in vivo testing and formal reporting required for preclinical regulatory clearance. VivaMARS leverages our industry-leading Panema software platform as well as our Panlab activity monitoring expertise. It is an excellent example of how we're able to leverage our expertise across all of Harvard Bioscience family. This system was developed with our CRO and pharma customer needs in mind and also meets their business needs to increase operating efficiencies, lowering costs and more importantly, reducing test cycle times to expand capacity and support their revenue growth. We're expecting our first VivaMARS shipment to a CRO customer later in this year. Finally, we'll be showcasing our new SoHo small animal model telemetry platform. SoHo is based on our industry-leading telemetry and Penema enterprise software platform and extends our leadership position with expanded capabilities such as concurrent multi-model testing in a more natural shared housing environment. As with VivaMARS, this platform is designed to meet customers' challenging business needs for lowering operating costs and shorter test cycle times to expand test capacity and drive more of their revenue growth. Now I'll turn the call over to Jennifer, our CFO, for a look at key financials. Jennifer?