How to Use CDISC’s ODM Standard for CRF Design
Over the last decade, our industry has become familiar with Clinical Data Interchange Standards Consortium…
Certara2024年9月25日
How Clinical Trial Technology Streamlines the Research Process
Learn how innovative clinical trial technology helps to revolutionize research & ensure the swift rollout…
Certara2024年9月25日
All You Need to Know About Non-CRF Data in Clinical Trials
We look at the role of non-CRF data in clinical trials, and best practices for…
Certara2024年9月16日
Why Should You Use LOINC Codes For SDTM?
2024年9月16日 In this blog, we take a detailed look at LOINC Codes and…
Certara2024年9月16日
The SDTM Mapping Process Simplified
SDTM mapping can be one of the most challenging programming problems in a clinical trial…
Certara2024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…
Certara2024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…
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 mandatory requirement of the FDA, and therefore a key submission deliverable for…
Certara2024年8月26日
