Beyond Compliance: How Novel Animal Welfare Initiatives Shape Better Science
Animal welfare investment at Scantox goes well beyond accreditation. AAALAC-certified facilities, a Culture of Care program, positive reinforcement training, and the newly opened indoor/outdoor facility combine to create study conditions in which welfare standards and scientific quality are built from the same foundation.
Join Mikkel Lykke Krarup, DVM, Chief Scientific Officer, Regulatory Toxicology at Scantox for “Beyond Compliance: How Novel Animal Welfare Initiatives Shape Better Science” on June 25, 2026 | 15:00 CEST, followed by a Q&A session.
Mikkel will walk through Scantox’s welfare program in practice: from the AAALAC and GLP foundation through Culture of Care, species-specific enrichment, specialized training, innovative techniques and facility design – and what each means for data quality and study outcomes.
Whether you are a study director, a toxicologist evaluating CRO animal welfare standards, or a preclinical development lead, this session offers a practical view of what welfare-driven science looks like at a leading European CRO.
Key Learning Objectives
- Understand the Culture of Care framework and how AAALAC accreditation underpins Scantox's approach to welfare-driven science.
- Explore the design principles behind Scantox’s indoor/outdoor facility and what they mean for stress reduction and study quality.
- Discover how positive reinforcement training enables large animals to complete specific procedures voluntarily, improving study conduct and data reliability.
- Examine the role of enrichment programs and daily human–animal interaction in reducing background variability and supporting GLP-quality data.
- Learn how veterinarian-led procedure refinement and an open staff culture make high welfare standards sustainable across studies and sites.
Who Should Attend
- Study directors and in-life scientists working with rodents, minipigs, dogs, or other large-animal species.
- Toxicologists and preclinical development leaders evaluating CRO partners for regulatory toxicology studies.
- Animal welfare officers, veterinarians, and laboratory animal scientists with 3Rs program responsibility.
- Regulatory affairs professionals assessing how facility accreditation supports IND/IMPD submissions.
- Project managers and outsourcing leads at biotech companies seeking CRO partners with strong welfare credentials.
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