Regulatory requirements for annotated CRFs made easy
aCRFs are a key submission deliverable for any clinical trial. In this blog, we break…
Gilbert HunterAugust 26, 2024
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
All you need to know about NCI, CDISC and SDTM controlled terminology
The use of controlled terminology (CT) is vital to successful clinical study build. In clinical…
CertaraAugust 13, 2024
Pinnacle 21 Non-CRF Data
Learn how Pinnacle 21 Non-CRF Data Exchange streamlines vendor data with collaborative spec design, automated…
CertaraAugust 9, 2024
A quick guide to implementing a Clinical Metadata Repository
Read our free guide to learn the three-step best practice process to implementing a Clinical…
CertaraAugust 7, 2024
A guide to CDISC standards used in clinical research
An overview of CDISC standards in the clinical research process. Learn about content standards, data…
Gilbert HunterJuly 29, 2024
Pinnacle 21 Enterprise analytics: Case studies from the field
In this blog, we look at some examples of how Pinnacle 21 Enterprise Analytics (P21E)…
CertaraJuly 15, 2024
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
How a top 10 pharma fought the rising tide of non-EDC data
Discover how a top pharma company used Pinnacle 21 Data Exchange to automate non-CRF data…
CertaraJune 17, 2024
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
