Managing Your FDA "483" Inspectional Observations 2017 is a webinar that covers topics such as:
- How to interpret the 483 - "How bad is it?"
- What the 483 means
- Responding to the FDA in writing
- Managing the 483 discussion with the FDA at the conclusion of the inspection
- What to expect during the next FDA inspection
- Use of a Corrective and Preventive Action program
Managing Your FDA "483" Inspectional Observations 2017 is intended for:
- FDA Consultants
- Manufacturers
- Regulatory Affairs Managers
- Legal Counsel
- Operations Directors
- Quality Assurance Staff