Ask the Experts
Insights Archive
Ask the Experts
Ask the Experts
Is it possible to make a PI’s name or institution confidential on a consent form?
Read More about Is it possible to make a PI’s name or institution confidential on a consent form?
Ask the Experts
How do I establish an IRB for reviewing clinical trials?
Read More about How do I establish an IRB for reviewing clinical trials?
Ask the Experts
What are the Blood Draw Guidelines for Phase 1 Clinical Trials?
Read More about What are the Blood Draw Guidelines for Phase 1 Clinical Trials?
Ask the Experts
Questions on Using Generic Recruitment Flyers at Clinical Trial Sites
Read More about Questions on Using Generic Recruitment Flyers at Clinical Trial Sites
Whitepapers
An Overview of the Recent SACHRP Recommendations Around Payments in Clinical Research
Read More about An Overview of the Recent SACHRP Recommendations Around Payments in Clinical Research
Ask the Experts
Have WCG IRBs adopted the 2018 revisions to the Common Rule for the Protection of Human Subjects?
Read More about Have WCG IRBs adopted the 2018 revisions to the Common Rule for the Protection of Human Subjects?
Ask the Experts
Guidance on genomic research with deceased patients
Read More about Guidance on genomic research with deceased patients
Ask the Experts
What is the IRB’s responsibility for the review of updated Investigator Brochures?
Read More about What is the IRB’s responsibility for the review of updated Investigator Brochures?
Ask the Experts