Regulatory Compliance
FDA & ICH
Assessing Potential Risks in the Consideration of IND Exemption Criteria
Blog Posts
Ethics in Clinical Research
Defining “Minimal Risk” in Clinical Research
Blog Posts
Ethics in Clinical Research
Which comes first – IRB or IBC approval?
Blog Posts
Cell & Gene Therapy
Is special safety equipment required for IBC approval?
Blog Posts
Ethics in Clinical Research
Do we need to submit screenshots of eCOA/ePRO diaries?
Blog Posts
Ethics in Clinical Research
Should Parents Be Allowed to View their Child’s Survey Responses?
Blog Posts
Clinical Trial Safety
WCG IRB Central and Institutional Site Relationships
Case Studies
Ethics in Clinical Research
Drafting a Research Plan for IRB Review and Research Conduct: Information That Must Be Included in a Clinical Trial Protocol
Whitepapers
Ethics in Clinical Research
What are the requirements for notifications of study closure at research sites?
Blog Posts
Ethics in Clinical Research