Certara Products Archives

Publication

A literature review of drug transport mechanisms during lactation

The literature review titled "A literature review of drug transport mechanisms during lactation," authored by…

CertaraJuly 7, 2024

Blog

3 Things You Should Know About ADaM Standards

Learn the key aspects of ADaM standards, including the difference between SDTM and ADaM and…

CertaraJuly 4, 2024

Blog

Future Clinical Study Design: CDISC, FHIR, OMOP, or Hybrid Model?

June 27, 2024 Advances in technology and changes to the regulatory environment have resulted in…

CertaraJune 27, 2024

Press Coverage

Adopting the Power of AI to Drug Development Projects: Making go/no-go decisions with MBMA and CODEx Clinical Outcome database

CertaraJune 26, 2024

Blog

ICH M12 Guidelines & Your Drug-Drug Interaction Package

We have provided an overview of the key changes to the ICH M12 drug-drug interaction…

CertaraJune 19, 2024

Case Study

How a top 10 pharma fought the rising tide of non-CRF data

Discover how a top pharma company used Pinnacle 21 Data Exchange to automate non-CRF data…

CertaraJune 17, 2024

Blog

Using Real World Data in Clinical Trial Submissions

We explore challenges & best practice recommendations to help you implement submission standards when using…

CertaraJune 17, 2024

Guide

A Best Practice Guide to CRF Design

Design quality, effective and reusable case report forms with our CRF Design Guide. Download the…

CertaraJune 7, 2024

Blog

Clinical trial data validation: When to transition from P21 Community to Enterprise

Technology is designed to help us live and work smarter. That is exactly what P21’s…

CertaraJune 7, 2024

Case Study

Streamlining Biotech Data Compliance and Management with Certara’s Phoenix Hosted

Discover how Certara's Phoenix Hosted streamlined data compliance and management for a biotech company, enhancing…

CertaraMay 31, 2024

Certara Products

A literature review of drug transport mechanisms during lactation

3 Things You Should Know About ADaM Standards

Future Clinical Study Design: CDISC, FHIR, OMOP, or Hybrid Model?

Adopting the Power of AI to Drug Development Projects: Making go/no-go decisions with MBMA and CODEx Clinical Outcome database

ICH M12 Guidelines & Your Drug-Drug Interaction Package

How a top 10 pharma fought the rising tide of non-CRF data

Using Real World Data in Clinical Trial Submissions

A Best Practice Guide to CRF Design

Clinical trial data validation: When to transition from P21 Community to Enterprise

Streamlining Biotech Data Compliance and Management with Certara’s Phoenix Hosted

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