Engaged. Knowledge. Application
Clinical Trial Protocols CONTENT Package
1. Clinical Trial Protocols: An Introduction (Reference Article)
Click here to view complimentary excerpt
2. Clinical Trial Protocols (PDF PowerPoint Training Presentation)
3. Clinical Trial Protocols (Trainer Instructional Notes)
1. Clinical Trial Protocols: An Introduction (Reference Article)
Click here to view complimentary excerpt
This eight (8) page article reviews fundamentals of the following subject matter content:
- The three (3) stages of the drug development process
- Clinical trial phases
- Specific 21 CFR regulations that apply to clinical studies
- Important parts of a clinical trial protocol
- The process for developing and submitting a clinical trial protocol
- Identifying roles and responsibilities of the clinical trial sponsor, clinical trial investigator and IRB specific to an approved clinical trial protocol
- Change control process as it applies to a clinical trial protocol
- Protocol amendments
- 21 CFR 312.30
- Protocol deviations
2. and 3. Clinical Trial Protocols (PDF PowerPoint Training Presentation & Trainer Instructional Notes)
14 Slide PDF PowerPoint Training Presentation based on the subject matter presented in reference content article above. This PDF readymade presentation provides "core" subject matter content, and allows you to customize specific information within your presentation. Trainer instructional notes, which contain 30+ discussion points related to the PowerPoint training presentation, are also included. Trainer instructional notes are designed to help focus your presentation on key pints, engage attendees and encourage their participation in your training.
Clinical Trial Protocols CONTENT Package is only $99.00
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