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

This webinar on Trial Master File (TMF) for clinical research sites will show how you can create an FDA compliant TMF to ensure that it will pass inspection by FDA investigators and QA Auditors.

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

Who Will Benefit:

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

Exhibitors

Madhavi Diwanji, MBA, CCRC is the President of MD Clinical Monitor. She has tremendous experience in the healthcare industry in various roles for the past 20 years. She is well rounded in all aspects of clinical trial as she has been instrumental in healthcare research with a primary focus on cardiology and oncology.

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