Charles River Laboratories (NYSE:CRL) Q4 2025 Earnings call February 18, 2026 08:30 AM ET Company ParticipantsBirgit Girshick - EVP and COOCasey Woodring - VP, Equity ResearchDave Windley - Managing DirectorElizabeth Anderson - Senior Managing DirectorEric Coldwell - Managing DirectorJames Foster - Chair, President and CEOLuke Sergott - Director - Healthcare Equity ResearchMichael Knell - VP and Chief Financial OfficerMichael Ryskin - Managing DirectorTodd Spencer - VP of Investor RelationsConference Call P ...

Charles River Laboratories (NYSE:CRL) Q4 2025 Earnings call February 18, 2026 08:30 AM ET Company ParticipantsBirgit Girshick - EVP and COOCasey Woodring - VP, Equity ResearchDave Windley - Managing DirectorElizabeth Anderson - Senior Managing DirectorEric Coldwell - Managing DirectorJames Foster - Chair, President and CEOLuke Sergott - Director - Healthcare Equity ResearchMichael Knell - VP and Chief Financial OfficerMichael Ryskin - Managing DirectorTodd Spencer - VP of Investor RelationsConference Call P ...

Charles River Laboratories (NYSE:CRL) Q4 2025 Earnings call February 18, 2026 08:30 AM ET Speaker12I would now like to turn the conference over to your host, Todd Spencer, Vice President of Investor Relations. Please go ahead.Speaker14Good morning, and welcome to Charles River Laboratories' fourth quarter and full year 2025 earnings and 2026 guidance conference call and webcast. This morning, I am joined by Jim Foster, Chair, President, and Chief Executive Officer, Birgit Girshick, Executive Vice President ...

Financial Data and Key Metrics Changes - The company reported revenue of $984.2 million in Q1 2025, a 2.7% decrease compared to the previous year, with an organic revenue decline of 1.8% [21][38] - The operating margin improved to 19.1%, an increase of 60 basis points year over year, primarily due to cost savings from restructuring initiatives [22][38] - Earnings per share were $2.34, reflecting a 3.1% increase from the same quarter last year [22][38] Business Segment Data and Key Metrics Changes - DSA revenue was $592.6 million, a decrease of 1.4% on an organic basis, driven mainly by lower revenue for discovery services [24] - RMS revenue was $213.1 million, a decrease of 2.5% on an organic basis, primarily due to timing of NHP shipments in China and lower revenue for the cell solutions business [28] - Manufacturing segment revenue was $178.5 million, a 2.2% decrease on an organic basis, driven by lower commercial revenue in the CDMO business [30] Market Data and Key Metrics Changes - The DSA backlog was $1.99 billion at the end of Q1, up slightly from $1.97 billion at year-end [24] - The net book-to-bill ratio improved to 1.04 times, the first time above one since the second half of 2022, driven by higher gross bookings from global biopharmaceutical clients [25][26] Company Strategy and Development Direction - The company is focused on expanding its non-animal platforms and investing in alternative methods to reduce animal testing, aligning with FDA initiatives [13][19] - The company plans to continue its strategic investments in areas central to the NAMS ecosystem, including organoid and organ-on-a-chip platforms [15] - A comprehensive strategic review is underway to evaluate initiatives for unlocking additional value, in collaboration with new board members and Elliott Investment Management [34][47] Management's Comments on Operating Environment and Future Outlook - Management noted continued signs of stabilization in the market despite uncertainties, with a cautious approach to the second half of the year [20] - The company modestly raised its 2025 revenue guidance by 100 basis points, expecting a 2.5% to 4.5% organic revenue decline [23][40] - Management emphasized the importance of scientific validation in the transition to NAMS and the need for a hybrid approach in drug development [11][19] Other Important Information - The company generated approximately $200 million in annual DSA revenue from NAMS, with expectations for meaningful growth over time [16] - The company has repurchased $350 million in shares during Q1 2025 as part of its capital allocation strategy [38] Q&A Session Summary Question: Thoughts on FDA guidance and mixed messaging - Management acknowledged the complexity of changes at the FDA and emphasized the ongoing development of NAMS, expressing optimism about leading clients in sync with regulatory agencies [52][54] Question: Use of biosimulation technologies - Management indicated that while biosimulation technologies are used in early drug discovery, their application in regulated toxicology is more complex and will require significant validation [59][60] Question: Areas of investment and M&A in NAMS - Management expressed interest in acquiring technologies that enhance drug development without compromising patient safety, highlighting past acquisitions and ongoing evaluations of potential opportunities [66][70] Question: Impact of FDA changes on long-term growth - Management stated that a refresh of long-term growth rates is necessary, considering the new FDA information, but refrained from providing specific numbers at this time [84] Question: Pricing environment comparison to past crises - Management noted that the current pricing environment is stable compared to the Great Recession, with better capacity management and less severe price pressure [86][87]

Financial Data and Key Metrics Changes - The company reported revenue of $984.2 million in Q1 2025, a 2.7% decrease compared to the previous year, with an organic revenue decline of 1.8% [20][21] - The operating margin improved to 19.1%, an increase of 60 basis points year over year, primarily due to cost savings from restructuring initiatives [21][38] - Earnings per share were $2.34, reflecting a 3.1% increase from the same quarter last year [21] Business Segment Performance - DSA revenue was $592.6 million, a decrease of 1.4% on an organic basis, driven mainly by lower revenue for discovery services [23] - RMS revenue was $213.1 million, a decrease of 2.5% on an organic basis, primarily due to timing of NHP shipments in China and lower revenue for the cell solutions business [28] - Manufacturing segment revenue was $178.5 million, a 2.2% decrease on an organic basis, driven by lower commercial revenue in the CDMO business [30] Market Data and Key Metrics Changes - The DSA backlog was $1.99 billion at the end of Q1, up slightly from $1.97 billion at year-end [24] - The net book to bill ratio improved to 1.04 times for the first time in over two years, driven by higher gross bookings from global biopharmaceutical clients [25] - Revenue from small and mid-sized biotech clients grew for the second consecutive quarter, while revenue from global biopharmaceutical clients declined [20][21] Company Strategy and Industry Competition - The company is focused on integrating non-animal methods (NAMS) into its business, aligning with FDA initiatives to reduce animal testing [6][12] - The company plans to continue investing in alternative methods and technologies, including partnerships and acquisitions, to enhance its capabilities in drug development [12][66] - The strategic planning committee will undertake a comprehensive review to evaluate initiatives for unlocking additional value [35] Management's Comments on Operating Environment and Future Outlook - Management noted continued signs of stabilization in the market despite uncertainties, including government funding cuts and a slower start for biotech funding [19] - The company has modestly raised its 2025 revenue guidance due to better-than-expected DSA performance, now expecting a 2.5% to 4.5% organic revenue decline [22][40] - Management emphasized the importance of patient safety and the gradual adoption of NAMS, indicating that the transition will be evolutionary rather than revolutionary [18][60] Other Important Information - The company generated approximately $200 million in annual DSA revenue from NAMS, with expectations for meaningful growth over time [15] - The company has made strategic investments in various alternative methods, including organoid and organ-on-a-chip platforms [14] - The company repurchased $350 million in shares during Q1 2025 as part of its capital allocation strategy [38] Q&A Session Summary Question: Thoughts on FDA guidance and mixed messaging - Management acknowledged the complexity of changes at the FDA and emphasized the ongoing development of NAMS, indicating that the focus on monoclonal antibodies is a logical starting point [50][54] Question: Use of biosimulation technologies - Management noted that while biosimulation technologies are used in early drug discovery, their application in regulated toxicology is more complex and will require significant validation [56][58] Question: Company's position in NAMS and potential M&A - Management expressed interest in acquiring technologies that enhance drug development without compromising patient safety, highlighting past acquisitions and ongoing evaluations of potential opportunities [63][66] Question: Impact of FDA changes on long-term growth - Management indicated that a comprehensive review of long-term growth rates will be conducted, considering the new FDA information and client feedback [78] Question: Pricing environment comparison to past downturns - Management noted that the pricing environment has improved slightly, driven by a favorable mix, and is not experiencing the same level of pressure as during the Great Recession [81][83]