Model-Based Meta-Analysis (MBMA), Quantitative Systems Pharmacology (QSP), and Advanced Modeling in Early Reimbursement Strategy On-Demand Webinar Model-Based Meta-Analysis (MBMA), Quantitative Systems Pharmacology (QSP), and Advanced Modeling in Early Reimbursement Strategy Watch this on-demand webinar to learn how model-based meta-analysis (MBMA), quantitative systems pharmacology (QSP), and…CertaraJanuary 22, 2026
Safety First: Uncovering the Clinical Risks Inside Your Compound Screening Data On-Demand Webinar Safety First: Uncovering the Clinical Risks Inside Your Compound Screening Data Learn how to interpret screening assay data to predict clinical off-target risk with ToxStudio® and…CertaraJanuary 13, 2026
New Approach Methodologies (NAMs): By the numbers GuideInfographic New Approach Methodologies (NAMs): By the numbers We outline today’s animal-use landscape, the rise of NAMs, & how the Non-Animal Navigator supports…CertaraDecember 10, 2025
New Approach Methodologies: Redefining Animal Testing Alternatives PodcastPress Coverage New Approach Methodologies: Redefining Animal Testing Alternatives Explore how New Approach Methodologies (NAMs) and advanced in silico and in vitro tools are…CertaraDecember 10, 2025
A Guide to the FDA Announcement to Phase Out Animal Testing for Drugs Guide A Guide to the FDA Announcement to Phase Out Animal Testing for Drugs The FDA is phasing out animal testing of new drugs. Learn how Certara’s Non-Animal Navigator™…CertaraNovember 17, 2025
Certara Study Shows Half of Americans Unaware of FDA/NIH Move to Phase Out Animal Testing of New Drugs Announcement Certara Study Shows Half of Americans Unaware of FDA/NIH Move to Phase Out Animal Testing of New Drugs Certara’s new survey findings show that 50% of Americans are unaware of FDA and NIH…CertaraNovember 12, 2025
Towards new approach methodologies for biological therapeutics: a novel model-informed metric to assess immunogenicity risk Publication Towards new approach methodologies for biological therapeutics: a novel model-informed metric to assess immunogenicity risk Immunogenicity poses a significant challenge in biotherapeutics development due to the formation of anti-drug antibodies…Danielle PillsburyNovember 7, 2025
In silico Safety and Toxicology assessment: ToxStudio® On-Demand Webinar In silico Safety and Toxicology assessment: ToxStudio® Discover how Certara’s ToxStudio align with FDA’s roadmap to reduce animal testing and transform preclinical…CertaraOctober 30, 2025
Move Away From Animal-Only Testing May Improve, Speed Rare Disease Research Press Coverage Move Away From Animal-Only Testing May Improve, Speed Rare Disease Research The article, "Move Away From Animal-Only Testing May Improve, Speed Rare Disease Research," explores a…Danielle PillsburySeptember 10, 2025
AI-driven drug discovery picks up as FDA pushes to reduce animal testing Press Coverage AI-driven drug discovery picks up as FDA pushes to reduce animal testing AI is revolutionizing drug discovery and safety testing as drug developers adopt these technologies in…CertaraSeptember 9, 2025