Page 4 | Certara

Podcast Press Coverage

New Approach Methodologies: Redefining Animal Testing Alternatives

Explore how New Approach Methodologies (NAMs) and advanced in silico and in vitro tools are…

CertaraDecember 10, 2025

Webinar

Implementing AI in Medical Writing: Prepare Today for Tomorrow’s Efficiency [Japanese Webinar]

CertaraDecember 10, 2025

Blog

7 key annotated CRF regulatory submission requirements you should know

Discover 7 key aCRF regulatory submission requirements for delivering high-quality annotated CRFs, including real-world examples…

Gilbert HunterDecember 10, 2025

Live Events

QSP Workshop 2026 in Japan & Korea – Mastering Scalable AI-enabled QSP modeling software, Certara IQ™

Japan: February 26, 2026 - 1:00 - 5:00 pm | Korea: Wednesday, March 4, 2026…

CertaraDecember 9, 2025

Podcast Press Coverage

On Virtual Twin® models in rare disease research, with Piet van der Graaf

Using Virtual Twin models in rare disease drug development can improve clinical trial design, regulatory…

CertaraDecember 9, 2025

Blog

Virtual Triplets: The Next Step in Personalized and Ethical Drug Development

Learn how virtual triplets, linking PBPK, QSP, and organ-on-a-chip technologies, are transforming model-informed drug development,…

CertaraDecember 9, 2025

Webinar

Why Upgrade to Marvin? Unlocking Speed, Accuracy, and Scientific Intelligence

Danielle PillsburyDecember 8, 2025

Fact Sheet

Expedited Pharmacometrics Regulatory Submissions

Certara delivers complete, compliant pharmacometric regulatory submission packages in just 4–6 weeks, eliminating the PMx…

CertaraDecember 8, 2025

Webinar

AI-Powered PK Reporting: From Days to Minutes

CertaraDecember 4, 2025

Announcement

Certara Cuts Pharmacometrics Submission Timelines in Half: New Expedited Service Accelerates Global Regulatory Filings

Certara launches an expedited Pharmacometrics (PMx) Regulatory Submission service that cuts submission timelines in half.

CertaraDecember 3, 2025

New Approach Methodologies: Redefining Animal Testing Alternatives

Implementing AI in Medical Writing: Prepare Today for Tomorrow’s Efficiency [Japanese Webinar]

7 key annotated CRF regulatory submission requirements you should know

QSP Workshop 2026 in Japan & Korea – Mastering Scalable AI-enabled QSP modeling software, Certara IQ™

On Virtual Twin® models in rare disease research, with Piet van der Graaf

Virtual Triplets: The Next Step in Personalized and Ethical Drug Development

Why Upgrade to Marvin? Unlocking Speed, Accuracy, and Scientific Intelligence

Expedited Pharmacometrics Regulatory Submissions

AI-Powered PK Reporting: From Days to Minutes

Certara Cuts Pharmacometrics Submission Timelines in Half: New Expedited Service Accelerates Global Regulatory Filings

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