pre-update Archives

Blog

Streamline your clinical trials with automated metadata management

When it comes to efficient clinical study build, content is king. Most importantly: metadata content.…

CertaraAugust 26, 2024

Blog

Regulatory requirements for annotated CRFs made easy

aCRFs are a mandatory requirement of the FDA, and therefore a key submission deliverable for…

CertaraAugust 26, 2024

Blog

Resmetirom: A pioneering NASH clinical program

Nonalcoholic fatty liver disease (NAFLD) is a condition wherein the liver stores excess fat. Nonalcoholic…

CertaraAugust 23, 2024

Press Coverage

Overcoming CMC Challenges in Cell and Gene Therapy: Part I

In this Manufacturing Chemist article, Certara's Drs. Hien Anh Bruno and Deven Shah discuss the…

CertaraAugust 23, 2024

Press Release

Certara to Participate in Upcoming Investor Conferences

RADNOR, Pa. — August 21, 2024 -- Certara, Inc. (Nasdaq: CERT), a global leader in…

CertaraAugust 21, 2024

Blog

Quantitative Systems Pharmacology (QSP) Modeling for Immunotherapy-induced Cytokine Release Syndrome

Cytokine Release Syndrome Cytokine release syndrome (CRS) is an inflammatory immune reaction that clinically manifests…

CertaraAugust 20, 2024

On-Demand Webinar

Navigating New Terrain: Joint Advice on FDA/EMA Compliance – Aligning with Evolving EU Regulations

Presentation Materials

CertaraAugust 20, 2024

On-Demand Webinar

Navigating New Terrain: The Impact of Evolving EU Regulations on Regulatory Affairs

Presentation Materials Don't miss Part 2 in the series Joint Advice on FDA/EMA Compliance…

CertaraAugust 20, 2024

On-Demand Webinar

Using Quantitative Systems Pharmacology (QSP) Modeling for Oncology Dose Optimization

The FDA’s Project Optimus initiative aims to reform dose optimization and selection for oncology therapies…

CertaraAugust 19, 2024

Blog

Automation in clinical trials: Why it’s essential for success

Many companies in the life sciences industry are slow to adopt new technologies. This is…

CertaraAugust 19, 2024

pre-update

Streamline your clinical trials with automated metadata management

Regulatory requirements for annotated CRFs made easy

Resmetirom: A pioneering NASH clinical program

Overcoming CMC Challenges in Cell and Gene Therapy: Part I

Certara to Participate in Upcoming Investor Conferences

Quantitative Systems Pharmacology (QSP) Modeling for Immunotherapy-induced Cytokine Release Syndrome

Navigating New Terrain: Joint Advice on FDA/EMA Compliance – Aligning with Evolving EU Regulations

Navigating New Terrain: The Impact of Evolving EU Regulations on Regulatory Affairs

Using Quantitative Systems Pharmacology (QSP) Modeling for Oncology Dose Optimization

Automation in clinical trials: Why it’s essential for success

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