Research Sites & Institutions
Hybrid & Decentralized Trials
What are the regulations for training home health individuals who are working remotely to collect study data?
Blog Posts
Series: Ask the IRB & IBC Experts
Should Consent Form updates be aligned with Investigator Brochure updates, or wait for next Protocol amendment?
Blog Posts
COVID-19
Part 4: Planning for Recovery: How Research Sponsors and Research Sites are Thinking Ahead to Restart Research
Whitepapers
WCG’s WIRB-Copernicus IRB Announces New Program to Facilitate IRB Review of Research Protocols for COVID-19 (Coronavirus) Vaccines and Therapies
News
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
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
Series: Ask the IRB & IBC Experts
Is it possible to make a PI’s name or institution confidential on a consent form?
Blog Posts
Clinical Trial Safety