How to satisfy regulatory concerns about EDC data integrity and site controls over its source records.
Joonhyuk Choi
Advertisement
Articles by Joonhyuk Choi
Study results using a quality-by-design method, risk-based monitoring, and real-time direct data entry.
Advertisement
Latest Updated Articles
Three-Pronged Approach to Optimizing Trial MonitoringPublished: June 1st 2014 | Updated:
eSource Records in Clinical ResearchPublished: April 16th 2015 | Updated:
- eSource Records in Clinical Research: Keeping it Simple
Published: August 1st 2015 | Updated:
Advertisement
Advertisement
Trending on Applied Clinical Trials Online
1
Thermo Fisher, Lundbeck Announce New OpenAI Partnerships Advancing AI in Drug Development
2
Building Broader Investigator Networks to Advance Global Breast Cancer Research
3
ACT Brief: AI Expands Global Site Leadership as Ozempic Shows Potential to Reverse Biological Age
4
dashClinical: Real-Time Participant Payments
5
.png "BioPharm International")
.png "Pharmaceutical Commerce"){kind=logo}
.png "Turbo Machinery Magazine")
.png){kind=spacer}
