Quality Systems are a fundamental aspect of all pharmaceutical and medical device firms. They are an expectation and regulated requirement. Exactly what constitutes a quality system is different depending on the firm and the culture. Defining quality systems and then tracing them properly back to the FDA definitions is paramount for compliance and regulatory inspection preparedness.
Why should you Attend: The reason for attending would be to gain a perspective on what the expectations of a quality system are as they applies to validation and the requirements of regulations for the pharmaceutical and medical device industries.
Areas Covered in the Session:
Who Will Benefit: