Recommendations for Adopting New Approach Methodologies to Reduce Animal Testing in Drug Development eBook Recommendations for Adopting New Approach Methodologies to Reduce Animal Testing in Drug Development Discover advanced regulatory writing strategies, global regulatory submission best practices, eCTD guidance, ICH M15 updates…Certara2026年7月7日
The Power of Modeling: Speed, Early De-Risking, and Regulatory Success for Forward-Thinking Sponsors On-Demand Webinar The Power of Modeling: Speed, Early De-Risking, and Regulatory Success for Forward-Thinking Sponsors Learn how PBPK and QSP modeling support faster drug development by enabling smarter dose selection,…Certara2026年7月1日
Building IND-Ready and Investor-Ready Development Programs On-Demand Webinar IND申請と資金調達に向けた開発プログラムの構築 Learn how emerging biotechs can build IND-ready, investor-ready development programs using Totality of Evidence, NAMs,…Certara2026年6月15日
The Modeling Advantage: How Forward-Thinking Sponsors Are Moving Faster, De-Risking Earlier, and Winning with Regulators On-Demand Webinar The Modeling Advantage: How Forward-Thinking Sponsors Are Moving Faster, De-Risking Earlier, and Winning with Regulators Learn how PBPK and QSP modeling support regulatory confidence, accelerate drug development, and align with…Certara2026年5月26日
FDA Rebuilding After DOGE Cuts: Former Regulators Speak Out Press Coverage FDA Rebuilding After DOGE Cuts: Former Regulators Speak Out Former FDA officials describe the impact of DOGE-era staffing cuts, lost expertise, and the challenges…Certara2026年5月15日
How to Leverage PBPK Modeling and Simulation in Drug Research and Development Guide How to Leverage PBPK Modeling and Simulation in Drug Research and Development Learn how PBPK modeling and simulation in drug research and development reduces clinical burden, supports…Certara2026年5月12日
BioSpace webinar: Streamlining Nonclinical Development with FDA NAMs On-Demand Webinar BioSpace webinar: Streamlining Nonclinical Development with FDA NAMs Learn how to apply FDA NAM guidance to streamline nonclinical development, support IND decisions, and…Certara2026年5月8日
How pharma can transition to non-animal studies for investigational drugs Blog 医薬品企業が治験薬の非動物試験へ移行するための方法 Pharma companies can ease the transition to non-animal studies for investigational drugs by leveraging NAMs…Certara2026年5月5日
From models to impact: What QSPC 2026 revealed about the future of drug development Blog From models to impact: What QSPC 2026 revealed about the future of drug development Explore Certara’s insights from QSPC 2026, including virtual patients, regulatory adoption, AI in QSP, and…Certara2026年4月28日
ToxStudio® Predictive Toxicology Software Fact Sheet ToxStudio® Predictive Toxicology Software Learn about ToxStudio: Predictive toxicology software to support prediction of drug-induced liver injury (DILI), QT…Certara2026年4月16日