How To Avoid FDA 483 s/ Warning Letters? What to Do If You Happen to Get One? 2015 is a webinar that covers topics such as:
- Causes of Form 483 / Warning Letter
- FDA Inspections - background
- Best Practices for Responding to 483
- Some recent results of companies failing to respond appropriately
- What to do if the responses fail
- Best Practices for Responding to Warning Letter
How To Avoid FDA 483 s/ Warning Letters? What to Do If You Happen to Get One? 2015 is intended for:
- Regulatory Affairs professionals
- CEOs
- IT
- Quality
- Small business owners
- Engineers
- Consultants
- GxP
