Certara Products Archives

Case Study

Dreaming big with standardization in clinical trial design – one biopharma’s metadata automation journey

This case study explores how one biopharma gets deeper insights & more informed decision making…

CertaraMay 13, 2024

Case Study

How one university overcame practical and cultural challenges to implement CDISC compliance

A US-based university with a nationally recognized academic health center implemented Clinical Data Interchange Standards…

CertaraMay 8, 2024

Guide

A Best Practice Guide to CDISC SDTM Mapping

Complete the form to book your no-obligation demo of Pinnacle 21 and experience the transformative…

CertaraMay 7, 2024

Blog

Why are Clinical Data Standards Essential for EDC and Non-EDC Data?

Clinical data standards are essential for both EDC & non-EDC data. Learn how study build…

CertaraApril 25, 2024

Announcement

Pinnacle 21 Releases New PMDA, FDA, NMPA Validation Engines

Pinnacle 21 by Certara announces the latest Validation Engines for submissions to Japan PMDA, US…

CertaraApril 23, 2024

Guide

CRF Design Checklist

Our free, downloadable CRF design checklist can help you design quality case report forms that…

CertaraApril 10, 2024

Blog

What Should a Clinical Metadata Repository Do?

April 4, 2024 As the clinical research industry moves towards more efficient and automated processes, clinical…

CertaraApril 4, 2024

Blog

Everything You Need to Know About CRFs in Clinical Trials

Read about the basics of CRFs and eCRF design, why annotated CRFs should be standardized…

CertaraMarch 26, 2024

On-Demand Webinar

The State of AI in In Silico Trials and Drug Development – The Practical Application of AI in QSP [APAC Webinar]

The proliferation of AI models and GPTs has revolutionized how the life sciences industry consumes…

CertaraMarch 20, 2024

On-Demand Webinar

Adding Quality Control & Validation to Drug Discovery with AI

The proliferation of powerful AI models, including GPTs, has revolutionized how the life sciences industry…

CertaraMarch 14, 2024

Certara Products

Dreaming big with standardization in clinical trial design – one biopharma’s metadata automation journey

How one university overcame practical and cultural challenges to implement CDISC compliance

A Best Practice Guide to CDISC SDTM Mapping

Why are Clinical Data Standards Essential for EDC and Non-EDC Data?

Pinnacle 21 Releases New PMDA, FDA, NMPA Validation Engines

CRF Design Checklist

What Should a Clinical Metadata Repository Do?

Everything You Need to Know About CRFs in Clinical Trials

The State of AI in In Silico Trials and Drug Development – The Practical Application of AI in QSP [APAC Webinar]

Adding Quality Control & Validation to Drug Discovery with AI

Newsletter sign up

Quick links

Solutions

Contact