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

Blog

Model-based meta-analysis (MBMA) at GSK: Real-world impact on strategy and trials

GSK shares real-world case studies on how Model-Based Meta-Analysis (MBMA) supports dose selection, virtual control…

CertaraJuly 31, 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

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

Guide

How to Create a Data Validation Plan in Clinical Trials

Download our guide to creating a data validation plan in clinical trials, the ultimate blueprint…

CertaraJuly 21, 2025

On-Demand Webinar

Needle in the Haystack: The Role of Data Fabrics in Successful AI Implementation

CertaraJuly 18, 2025

Webinar

Pirana Tips and Tricks – Report Object Generation in Pirana

CertaraJuly 1, 2025

Blog

The reference-scaled average bioequivalence (RSABE) approach

We examine the Reference-scaled Average Bioequivalence (RSABE) approach for generic drug development and how it…

CertaraJuly 1, 2025

Blog

5 clinical development challenges model-based meta-analysis (MBMA) helps address

June 30, 2025 Drug development is increasingly defined by its complexity. Teams must navigate rising…

CertaraJune 30, 2025

Blog

Maintain & adapt pharma market access digital tools using feedback

Maintain the credibility of your pharma market access digital tools through continuous updates based on…

CertaraJune 30, 2025

Certara Products

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

Model-based meta-analysis (MBMA) at GSK: Real-world impact on strategy and trials

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

Three Approaches to AI Adoption in Regulatory Writing

How to Create a Data Validation Plan in Clinical Trials

Needle in the Haystack: The Role of Data Fabrics in Successful AI Implementation

Pirana Tips and Tricks – Report Object Generation in Pirana

The reference-scaled average bioequivalence (RSABE) approach

5 clinical development challenges model-based meta-analysis (MBMA) helps address

Maintain & adapt pharma market access digital tools using feedback

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