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
Why cancer drug programs need human mass balance studies
Historically, drug programs for oncology and other rapidly fatal diseases didn’t include mass balance studies…
Certara2024 年 9 月 23 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
What Are SDTM Supplemental Qualifiers?
A detailed look at data that exists out with SDTM variables, known as SDTM supplemental…
Certara2024 年 9 月 16 日
4 Ways That Mechanistic Modeling Accelerates Bispecific (and Multispecific) Antibody Drug Development
With nine FDA-approved drugs today, 100+ in clinical development and several hundred in the preclinical…
Certara2024 年 9 月 12 日
《降低通胀法案》对生物类似药市场有何影响？
The Inflation Reduction Act (IRA), one of the key legislative achievements the Biden-Harris administration, aims…
Certara2024 年 8 月 27 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
