As regulators phase out animal testing, biosimulation and AI emerge as the future of drug development
“Most consumers say testing medicines on animals is unethical, but they also believe it is the only way to ensure safety and efficacy,” said William F. Feehery, CEO. “Certara has been developing new approach methodologies (NAMs) like biosimulation for 25 years, and these tools are now being adopted globally. NAMs not only reduce reliance on animal models but also enable faster, safer, and more ethical development of new therapies.”
“Animal testing has long been how the public learns to trust that new medicines are safe and effective,” said Joshua Apgar, VP and Head of QSP Software. “The survey data reveal a critical education gap around next-generation approaches. Closing that trust gap will be essential, and it begins by ensuring transparency and communication about how alternative methods like biosimulation already provide the rigorous evidence regulators require.”
Survey Methodology
The survey was commissioned by Certara and conducted by Dynata, the world’s largest first-party data company. The survey was conducted in September 2025 among 1,000 U.S. consumers 18 years and older to understand the consumer sentiment on animal testing in pharmaceutical development and delivery.
About Certara
Certara accelerates medicines using proprietary biosimulation software, technology and services to transform traditional drug discovery and development. Its clients include more than 2,400 biopharmaceutical companies, academic institutions, and regulatory agencies across 70 countries. Visit us at www.certara.com.
Certara contact:
Sheila Rocchio
[email protected]
Media contact:
Alyssa Horowitz
[email protected]
Are you prepared for the FDA’s phase out of animal tests for mAbs?
Certara is ready to support the biopharmaceutical industry with a comprehensive offering of advanced modeling tools and development expertise that directly align with the FDA’s vision for the future of drug development.


