Trial Master File for Research Sites: Can You Pass FDA Inspection?
| Date: | 27-Jun-12 to 27-Jun-12 |
| Location: | Online Webinar / California / United States |
| Category: | Education Conferences & Trade Fairs |
Why Should You Attend:
Your clinical trial has zero chance of passing an FDA inspection or QA audit if your Trial Master File (TMF) is not in order.
The FDA frequently states that if compliance isn't documented, it didn't happen. Your TMF serves as living proof that you are adhering to GCP, and that your quality system is in a state of control.
Visitors
This webinar will provide valuable assistance to all personnel in:
- Clinical Research Manager
- Clinical Research Coordinators
- Clinical Research Associates
- Clinical Trial Investigators
- Administrative managers in charge of Clinical Research
- Regulatory, Compliance Associates and Managers
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