Trial Master File for Research Sites: Can You Pass FDA Inspection? - Clinical Webinar By ComplianceO (Clinical)

Venue: Online Event

Location: Palo Alto, California, United States

Event Date/Time: May 12, 2011 End Date/Time: May 12, 2011
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In this webinar, you will get guidance on the TMF. Learn the steps to take throughout a trial to ensure your TMF will pass inspection by FDA investigators and QA auditors.

Areas Covered in the Seminar:

- Documents that should, and should not, make up a Trial Master File.
- Maintenance and quality control of the TMF.
- Start smart—the steps to take from Day One to - create a compliant and useful TMF.
- Red flags that scream "noncompliance".
- Common pain points that you can expect to encounter, and how to keep them from driving your TMF into noncompliance.
- Note to File (NTF).
- CRA contributions to and adequate monitoring of the investigator TMF.

Note: Use these promocode(117660) for 10% discount.


Online Event
2600 E. Bayshore Road
Palo Alto
United States