Equipment Qualification and Process Validation 2019

Equipment Qualification and Process Validation 2019 is a webinar dedicated to FDA requirements for qualification and validation.

Topics

• Equipment Qualification
• General FDA GMP information requalification and validation
• Manufacturing and Cleaning Process Validation
• Computer System Qualification and Part 11

Who should Attend

• 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