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Basics of Good Clinical Practices for Clinical Research Coordinators
| Objective: | To introduce, apply, and analyze internationally accepted guidelines for clinical research on humans, including those of the International Conference on Harmonization (ICH) and the Food and Drug Administration (FDA). |
| Selected Topics: | Focus on Primary CRC Responsibilities, Document Management and Ethics Exercise in Source Documentation and Adverse Events Exercise in Study Conduct Guidelines for Trial Document Completion and Acceptance |
| Audience: | Clincal research coordinators |
