Regulatory Compliance
FDA & ICH
Sunsetting FDA Enforcement Discretion of Laboratory Developed Tests
Blog Posts
Regulatory Compliance
How WCG Is Preparing for FDA Harmonization with the Common Rule
Blog Posts
Regulatory Compliance
Dietary Supplements: Regulations in Research Studies and IRB Considerations
Blog Posts
Ethics in Clinical Research
What Information Must Be Included in the Cost Section of an Informed Consent Form?
Blog Posts
Ethics in Clinical Research
A Review Of The Regulatory Landscape for In Vitro Gametogenesis
Blog Posts
Ethics in Clinical Research
Why Was My Research Submission/Protocol Deferred? And What Should I Do?
Blog Posts
Biosafety
How New Changes to the NIH Guidelines Will Impact IBC Review
Blog Posts
Ethics in Clinical Research
If My Study Includes Approved Drugs, When Do the Risks of Those Drugs Need to Be Disclosed in the Consent Form?
Blog Posts
Diversity & Inclusion
FDA’s Path Toward Diversity in Clinical Trials: The DEPICT Act and Sponsor Responsibility
Whitepapers
Ethics in Clinical Research