Ethics, Compliance and Regulatory Guidance
CenterWatch | Insights
Safeguarding Participant Rights and Safety Requires Collaboration: Exploring the Duties of Sponsors, Sites and IRBs
Blog Posts
CenterWatch | Insights
Diversity Action Plans Will Soon Be Mandatory for Clinical Trials
Blog Posts
CenterWatch | Insights
Understanding the FDA’s new proposed regulations on human subject research and their impact on your clinical trial plans
Videos
CenterWatch | Insights
Assessing Potential Risks in the Consideration of IND Exemption Criteria
Blog Posts
CenterWatch | Insights
Defining “Minimal Risk” in Clinical Research
Blog Posts
CenterWatch | Insights
Should Parents Be Allowed to View their Child’s Survey Responses?
Blog Posts
CenterWatch | Insights
Adults with Limited Capacity to Consent to Research
Blog Posts
CenterWatch | Insights
Subject Injury Language for Clinical Trial Agreements – Details You Shouldn’t Overlook in Subject Injury Provision
Blog Posts
CenterWatch | Insights
Ethical and Regulatory Considerations in Patient-to-Patient-Referral Recruitment Plans
Whitepapers
CenterWatch | Insights