How to handle a regulatory inspection to avoid FDA-483 issues 2014 is a webinar that covers topics such as:
- Good record keeping for GMP and non-GMP studies
- Determine the sequences of an inspection
- Presenting clear and concise information
- Establish a process of handling an inspection
- Keep clear and concise records of observations
- Train your personnel to handle an inspection
- Determine your compliance weaknesses
How to handle a regulatory inspection to avoid FDA-483 issues 2014 brings together:
- Regulators
- Analytical chemists
- Researchers who are involved in inspections
