TrialAssure & Certara Joint Webinar: Authoring Clinical Documents with Downstream Regulatory Requirements in Mind
Watch our on-demand webinar from Certara and TrialAssure to learn how to author clinical documents…
Certara2025 年 9 月 10 日
The Pursuit of Certainty: Integrated Evidence and the evolving drug development and reimbursement landscape
Watch leading experts from Pfizer, Merck, Amicus, and Certara discuss how Integrated Evidence can bridge…
Certara2025 年 9 月 3 日
Designing a High-Value Drug Development Program: From Concept to First-in-Human (FIH)
Learn to design drug development programs for First-in-Human (FIH) success with biomarkers, PK/PD modeling, and…
Certara2025 年 8 月 29 日
Streamline Table Creation with AI-Specialized for Regulatory Writers
Learn how AI-powered CoAuthor™ transforms table creation for regulatory and medical writers. Watch our free…
Certara2025 年 8 月 27 日
Certara Integral: The Master Data Repository Powering Efficient and Collaborative PK/PD Workflows
Charles River improved its global pharmacokinetics workflows by adopting Certara’s Integral as a central data…
Certara2025 年 8 月 27 日
Blueprint for Biotech Success: De-risking Early Development to Secure Long-Term Value
Discover strategies to cut risk, speed timelines, and boost investor confidence in early biotech development.
Certara2025 年 8 月 21 日
ToxStudio®: In silico tools to accelerate toxicology assessments
Watch to explore ToxStudio—in silico toxicology platform designed to address key preclinical safety challenges.
Certara2025 年 8 月 19 日
The Many Challenges of Patient Narrative Writing | RAPS Sponsored Webinar
Watch Certara’s RAPS-sponsored on-demand webinar to learn how automation and expert strategies simplify patient narrative…
Certara2025 年 8 月 18 日
Differences between eCTD 4.0 and eCTD 3.2.2 Submissions – What You Need to Know
Access our on-demand webinar to explore the key differences between eCTD 4.0 and eCTD 3.2.2.…
Certara2025 年 8 月 11 日
