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Online Educational Library
Regulatory Science Symposium: Monitoring and Auditing Session 1: Introduction to Monitoring, Auditing, and FDA Inspections & GCP (2016)
In this series, we will discuss regulatory complexities regarding clinical trials.
regulatory science, responsible conduct of researchRegulatory Science Symposium: Monitoring and Auditing Session 3: Auditing GCP Systems for Data Integrity (2016)
In this series, we will discuss data integrity, GCP systems, regulatory framework enforcement, and auditing for data integrity
regulatory science, responsible conduct of researchRegulatory Science Symposium: Monitoring and Auditing Session 4: Sponsor Audits: Data Handling and Reports (2016)
In this series, we will discuss what a sponsor does with data after a clinical trial finishes at a site, focusing on audits.
regulatory science, responsible conduct of researchRegulatory Science Symposium: Monitoring and Auditing Session 2: FDA Inspections - Getting Ready (2016)
In this series, we will discuss regulatory complexities regarding clinical trials.
regulatory science, responsible conduct of researchRegulatory Science Symposium: Monitoring and Auditing Session 5: Workshop: GCP Audit Process and Checklist Scope (2016)
In this series, you will be asked to develop an audit plan and audit checklist for GCP Compliance.
regulatory science, responsible conduct of research