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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.
Beyond simply being a get out of jail free card, a well-maintained TMF can make trial management easier; with a typical TMF containing thousands of pages of documentation, you could easily save, or lose, hundreds of hours over the life of a trial searching for individual pieces of knowledge.
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.
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
- Research Site Personnel involved in set-up and maintenance of any trial TMF
- Quality Assurance of Research Sites
- Research Site Personnel in Charge of Policy Development and Maintenance
