This webinar will provide understanding of FDA and ISO 13485 requirements for process validation and how to implement them.
Why Should You Attend:
Process validation is a requirement but knowing when to validate or revalidate a process is essential. If you do not validate you risk enforcement actions such as fines or recalls, but too much validation is costly in both time and money.
This webinar will cover the basics of this important topic for those who are new to quality or new to process validation. It will:
- Cover the requirements for process validation from FDA cGMP and ISO 13485.
- Discuss when process validation and revalidation are necessary or desirable.
- Provide an outline of equipment qualification.
- Provide an overview of what is required for process validation.