Equipment Qualification and Process Validation 2019 is a webinar dedicated to FDA requirements for qualification and validation.
Equipment Qualification and Process Validation 2019 covers topics such as:
- Equipment Qualification
- General FDA GMP information requalification and validation
- Manufacturing and Cleaning Process Validation
- Computer System Qualification and Part 11
Equipment Qualification and Process Validation 2019 is intended for:
- Personnel responsible for computer system qualification
- Personnel responsible for equipment qualification
- Personnel responsible for cleaning validation
- Personnel responsible for manufacturing process validation
- Quality Professionals
- Regulatory Affairs, Regulatory Compliance
