Reducing your Exposure to a GMP FDA Warning Letter 2015 is a webinar that covers topics such as:
- What should always exist during an inspection?
- How to prepare for inspections
- How can you reduce your risk for a Warning Letter?
- What systems will get the greatest attention from a regulatory agency?
- What do you do after receiving a 483 observation?
- How does past regulatory history impact your future?
- How do you determine if a serious risk exists?
Reducing your Exposure to a GMP FDA Warning Letter 2015 is intended for attendees from:
- Quality Assurance
- Quality Control
- Laboratory
- Production
- Distribution and even Development personnel that are Supervisory
- Warehousing
- Management or directly performing regulatory related activities or support
