Regulatory Science Symposium: "Ensuring Clinical Trial Compliance" Session 7 - Wrap-up

Regulatory & Quality Sciences
Study & Site Management
Research & Study Conduct

Regulatory Science Symposium: "Ensuring Clinical Trial Compliance" Session 6 - Bioresearch Monitoring Program (BIMO), Good Clinical Practice Inspections, Compliance and Warning Letters

Regulatory & Quality Sciences
Study & Site Management
Research & Study Conduct

Regulatory Science Symposium: "Ensuring Clinical Trial Compliance" Session 5 - Good Distribution Practices: Application of supply chain management and quality management systems

Regulatory & Quality Sciences
Study & Site Management
Research & Study Conduct

Regulatory Science Symposium: "Ensuring Clinical Trial Compliance" Session 4 - Good Clinical Practice for Site Audits

Regulatory & Quality Sciences
Study & Site Management
Research & Study Conduct

Regulatory Science Symposium: "Ensuring Clinical Trial Compliance" Session 3 - Sponsor Audits: Data Handling and Reports

Regulatory & Quality Sciences
Study & Site Management
Research & Study Conduct

Regulatory Science Symposium: "Ensuring Clinical Trial Compliance" Session 2 - Good Clinical Practice (GCP) and FDA Inspection Preparation

Regulatory & Quality Sciences
Study & Site Management
Research & Study Conduct

Regulatory Science Symposium: "Ensuring Clinical Trial Compliance" Session 1 - Welcome

Dr. Eunjoo Pacifici, Chair of the Department of Regulatory and Quality Sciences, welcomes attendees to the symposium.

Regulatory & Quality Sciences
Study & Site Management
Research & Study Conduct

NIH Funding Acknowledgment: Important - All publications resulting from the utilization of SC CTSI resources are required to credit the SC CTSI grant by including the NIH funding acknowledgment and must comply with the NIH Public Access Policy.