Overview:
Covers the processes required to prepare a site for inspection before a regulator arrives. Thereafter how to conduct the process once the regulator is on site.
Why you should Attend:
Many companies are under preparing for regulatory inspections and as a result are being caught out with avoidable citations or negative results that could affect a licensing situation.
This wastes both time which is significant and raises the cost of getting the product either into clinical trials or licensed for the market.
This reduces the uncertainty around moving a product forward through the developmental process and into the market place.
Areas Covered in the Session:
- Site preparation
- Includes constructing an audit team and a document repository team
- Covers preparation of answers for questions
- Covers who should run the process and why
- Covers who should respond to questions
- Covers how to respond to questions and dos and don’ts
- Cover the meetings and close out meeting
- Covers post audit actions
Who Will Benefit:
- Manufacturing Staff
- QA and QC Staff
- Project Managers
- Senior Management Team