What Are SDTM Supplemental Qualifiers?
A detailed look at data that exists out with SDTM variables, known as SDTM supplemental…
CertaraSeptember 16, 2024
Define.xml Submission Checklist
Learn how to create a compliant Define.xml submission package with our Define.xml submission checklist, and…
CertaraAugust 29, 2024
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
Regulatory requirements for annotated CRFs made easy
aCRFs are a key submission deliverable for any clinical trial. In this blog, we break…
CertaraAugust 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…
CertaraJuly 29, 2024
