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…
Simona Colucci2024 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…
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
The 25th Annual Simcyp Consortium Meeting
Every year, the Consortium—comprising over 30 leading biopharmaceutical companies—convenes to discuss Physiologically Based Pharmacokinetic (PBPK)…
Simona Colucci2024 年 9 月 1 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
Waiving clinical studies & accelerating drug development for kinase inhibitor drugs
Whether you're in pre, early, or late clinical stages, this eBook offers real-world insights into…
Simona Colucci2024 年 8 月 28 日
PBPK Applications (MIFD) Using the Simcyp™ Simulator
Explores strategies, regulatory validation, and solutions in small-molecule human Physiologically Based Pharmacokinetic modeling (PBPK).
Simona Colucci2024 年 8 月 28 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
生命科学行业的许多公司在采用新技术方面进展缓慢。This is…
Simona Colucci2024 年 8 月 19 日
