Ethics, Compliance and Regulatory Guidance
CenterWatch | Insights
The FDA Accepts ICH E11A on Pediatric Extrapolation: How Does This Impact Your Pediatric Study?
Blog Posts
CenterWatch | Insights
Compounded Drugs in Research: Navigating IND Exemptions and Current Regulations
Blog Posts
CenterWatch | Insights
Answering FAQs on HIPAA & PHI: Protect Participants’ Privacy & Ensure Compliance
Blog Posts
CenterWatch | Insights
Noncompliance: Now What? CAPA Principles and Best Practices in Clinical Research
Blog Posts
CenterWatch | Insights
The DEI Mandate: What’s on the Horizon and What’s Needed for IRB and Recruitment Processes (Part 1 of 2)
Videos
CenterWatch | Insights
Cancer Clinical Trial Eligibility Criteria: Washout Periods and Concomitant Medications Guidance for Industry, IRBs, and Clinical Investigators
Blog Posts
CenterWatch | Insights
Cancer Clinical Trial Eligibility Criteria: Performance Status Guidance for Industry, IRB, and Clinical Investigators
Blog Posts
CenterWatch | Insights
Reconsenting Phrase Revisions
Blog Posts
CenterWatch | Insights
Navigating the Future: A Multi-Stakeholder Approach to Ethical AI Integration in Clinical Trials
Blog Posts
CenterWatch | Insights