Biotech Leaders
Series: Ask the IRB & IBC Experts
What documentation is needed to prove a parent’s legal authority to consent for a child’s participation in research?
Blog Posts
Clinical Endpoints
People, Process and Technology: The Right Combination for Successful Expert Committees
Podcasts
COVID-19
IRB Experts Offer Advice for Changing Research Landscape
Articles
COVID-19
Part 10: Unique Challenges and Opportunities for Emerging Biopharma Companies with Focused Pipelines
Whitepapers
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 10: Unique Challenges and Opportunities for Emerging Biopharma Companies with Focused Pipelines
Videos
COVID-19
Part 3: Evaluating Study Status and Leveraging Data Monitoring Committees to Make Study Decisions
WhitepapersWCG’s WIRB-Copernicus IRB Announces New Program to Facilitate IRB Review of Research Protocols for COVID-19 (Coronavirus) Vaccines and Therapies
News
Clinical Endpoints