Demystifying CDISC, SDTM, and ADaM
Breaking down the basics of CDISC’s CDASH, SDTM and ADaM standards, to help you understand…
CertaraMay 22, 2024
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…
CertaraMay 19, 2024
Dreaming big with standardization in clinical trial design – one biopharma’s metadata automation journey
This case study explores how one biopharma gets deeper insights & more informed decision making…
CertaraMay 13, 2024
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…
CertaraMay 8, 2024
How Chinese CRO, Zhejiang Longcharm Biomedical Technology Uses Pinnacle 21 Enterprise to Optimize Sponsors’ Non-clinical and Clinical Regulatory Affairs
Learn how one CRO uses Pinnacle 21 to optimize sponsors’ clinical regulatory affairs, saving time…
CertaraMay 6, 2024
Why are Clinical Data Standards Essential for EDC and Non-EDC Data?
Clinical data standards are essential for both EDC & non-EDC data. Learn how study build…
CertaraApril 25, 2024
Pinnacle 21 Releases New PMDA, FDA, NMPA Validation Engines
Pinnacle 21 by Certara announces the latest Validation Engines for submissions to Japan PMDA, US…
CertaraApril 23, 2024
CRF Design Checklist
Our free, downloadable CRF design checklist can help you design quality case report forms that…
CertaraApril 10, 2024
What Should a Clinical Metadata Repository Do?
April 4, 2024 As the clinical research industry moves towards more efficient and automated processes, clinical…
CertaraApril 4, 2024
