The SDTM Mapping Process Simplified
SDTM mapping can be one of the most challenging programming problems in a clinical trial…
Simona Colucci2024年9月16日
What Are SDTM Supplemental Qualifiers?
We touched on the SDTM supplemental qualifier in the SDTM mapping process simplified. In this…
Simona Colucci2024年9月16日
Define.xml Submission Checklist
Learn how to create a compliant Define.xml submission package with our Define.xml submission checklist, and…
Simona Colucci2024年8月29日
Streamline your clinical trials with automated metadata management
When it comes to efficient clinical study build, content is king. Most importantly: metadata content.…
Simona Colucci2024年8月26日
Regulatory requirements for annotated CRFs made easy
aCRFs are a mandatory requirement of the FDA, and therefore a key submission deliverable for…
Simona Colucci2024年8月26日
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…
Simona Colucci2024年8月19日
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…
Simona Colucci2024年8月13日
A quick guide to implementing a Clinical MDR
Read our free guide to learn the three-step best practice process to implementing a Clinical…
Simona Colucci2024年8月7日
A guide to CDISC standards used in clinical research
The Clinical Data Interchange Standards Consortium (CDISC) is dedicated to helping improve medical research through…
Simona Colucci2024年7月29日
Pinnacle 21 Enterprise Analytics: Case Studies from the Field
In this blog, we look at some examples of how Pinnacle 21 Enterprise Analytics (P21E)…
Certara2024年7月15日
