Define.xml Submission Checklist
Learn how to create a compliant Define.xml submission package with our Define.xml submission checklist, and…
Certara2024 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.…
Certara2024 年 8 月 26 日
Regulatory requirements for annotated CRFs made easy
aCRFs are a key submission deliverable for any clinical trial. In this blog, we break…
Certara2024 年 8 月 26 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…
Certara2024 年 8 月 13 日
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…
Certara2024 年 8 月 7 日
A guide to CDISC standards used in clinical research
An overview of CDISC standards in the clinical research process. Learn about content standards, data…
Certara2024 年 7 月 29 日
Future Clinical Study Design: CDISC, FHIR, OMOP, or Hybrid Model?
2024 年 6 月 27 日 Advances in technology and changes to the regulatory environment have resulted in…
Certara2024 年 6 月 27 日
Leveling Up SDTM Validation with the Magic of Data Managers
In this abstract, Julie Ann Hood and Jennifer Manzi look at how you can improve…
Certara2024 年 5 月 19 日
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…
Certara2024 年 5 月 8 日
