Trial Master File for Research Sites: Can You Pass FDA Inspection? - Clinical Webinar By ComplianceO (Clinical)
Venue: Online Event
|Event Date/Time: May 12, 2011||End Date/Time: May 12, 2011|
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 smartâ€”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.
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