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Curriculum
- 1 Section
- 8 Lessons
- Lifetime
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- Fundamentals of Clinical Research Associate8
- 1.1Module 01: Introduction to Clinical Research and Medicines Development
- 1.2Module 02: Medicines Development Process and Good Clinical Practice (GCP)
- 1.3Module 03: Clinical Trial Design and Roles & Responsibilities
- 1.4Module 04: Patient Protection and Adverse Events
- 1.5Module 05: Selecting and Initiating Clinical Trial Sites
- 1.6Module 06: Monitoring and Closing Clinical Trial Sites
- 1.7Module 07: Investigational Medicinal Product (IMP) and Data Management
- 1.8Module 08: Regulatory Environment in the EU and USA
Module 07: Investigational Medicinal Product (IMP) and Data Management
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