Med/Sci
COVID-19
Part 3: Evaluating Study Status and Leveraging Data Monitoring Committees to Make Study Decisions
Whitepapers
WCG’s WIRB-Copernicus IRB Announces New Program to Facilitate IRB Review of Research Protocols for COVID-19 (Coronavirus) Vaccines and Therapies
News
Clinical Endpoints
AIMS: Our Proprietary Web-Based Adjudication System
Videos
Ethics in Clinical Research
What are the requirements for parental permission (consent) in studies involving children?
Blog Posts
What ethical safeguards are needed for research involving observation of group behavior?
Blog Posts
An Inside Look at the Role of Data Monitoring Committees with Dr. Jonathan Seltzer
Podcasts
Regulatory Compliance
How do I handle a deviation in the use of blood specimens collected outside the timeframe?
Blog Posts
Questions on the FDA’s 30-Day IND Review Period and IRB Approval
Blog Posts
Clinical Trial Safety
WCG IBC Services
Solution Overviews