On-Demand Webinar Archives

On-Demand Webinar

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…

CertaraAugust 18, 2025

On-Demand Webinar

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.…

CertaraAugust 11, 2025

On-Demand Webinar

De-risking DDI Management during Clinical Trials: Introducing DIDB’s Concomitant Meds Navigator

Watch the on-demand presentation covering how the DIDB® Concomitant Meds Navigator empowers clinical development teams…

CertaraAugust 5, 2025

On-Demand Webinar

Mechanistic Models at the Regulatory Frontier: Insights from EMA’s Qualification of the Simcyp® Simulator

The European Medicines Agency (EMA) formally qualified Certara’s Simcyp® Simulator, marking the first and only…

CertaraAugust 4, 2025

On-Demand Webinar

Understanding Antibody-Drug Conjugates (ADCs) Pharmacokinetics From NCA to Population PK Approaches

CertaraAugust 1, 2025

On-Demand Webinar

Insights Without Animals: Leveraging Human-on-a-Chip & PBPK Modeling

CertaraJuly 29, 2025

On-Demand Webinar

MIDD Strategies for Preclinical and Clinical Translation: A Collaboration Between Clinical Pharmacologists and Modeling Disciplines

Learn how clinical pharmacologists and modeling experts collaborate to improve preclinical-to-clinical translation.

CertaraJuly 29, 2025

On-Demand Webinar

Boosting Confidence in Drug Discovery with PBPK

Explore Simcyp Discovery Version 2 updates to boost early-stage drug development.

CertaraJuly 25, 2025

On-Demand Webinar

2025 Virtual SEND Explorer® UGM

CertaraJuly 24, 2025

On-Demand Webinar

Three Approaches to AI Adoption in Regulatory Writing

Certara experts discuss AI adoption in medical writing: learn practical models, GenAI & SCA integration,…

CertaraJuly 23, 2025

On-Demand Webinar

The Many Challenges of Patient Narrative Writing | RAPS Sponsored Webinar

Differences between eCTD 4.0 and eCTD 3.2.2 Submissions – What You Need to Know

De-risking DDI Management during Clinical Trials: Introducing DIDB’s Concomitant Meds Navigator

Mechanistic Models at the Regulatory Frontier: Insights from EMA’s Qualification of the Simcyp® Simulator

Understanding Antibody-Drug Conjugates (ADCs) Pharmacokinetics From NCA to Population PK Approaches

Insights Without Animals: Leveraging Human-on-a-Chip & PBPK Modeling

MIDD Strategies for Preclinical and Clinical Translation: A Collaboration Between Clinical Pharmacologists and Modeling Disciplines

Boosting Confidence in Drug Discovery with PBPK

2025 Virtual SEND Explorer® UGM

Three Approaches to AI Adoption in Regulatory Writing

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