Improve your knowledge surrounding the proper conduct of clinical research with human subjects. You’ll learn more about the fundamental requirements for major markets, the role of the informed consent process, types and phases of clinical trials and protocol development, roles and responsibilities of parties involved in clinical research and issues related to trial management and safety monitoring.
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Products included in this bundle:
Online Course: Good Clinical Practice (GCP)
This online course is accessible for three months from the date of purchase.
- Lesson 1: Overview of Good Clinical Practices
- Lesson 2: GCP in the Real World
- Lesson 3: GCP Roles and Responsibilities
2–4 Hours | 2 RAC Credits
Online Course: Understanding and Managing the US Clinical Trial Process
This online course is accessible for three months from the date of purchase.
- Lesson 1: Foundations of Clinical Trials
- Lesson 2: Code of Federal Regulations Related to Clinical Trials
- Lesson 3: Structuring a Clinical Trial
- Lesson 4: Maintenance and Monitoring
- Lesson 5: Clinical Trial Data
4–8 Hours | 4 RAC Credits