Building a Sustainable Validation Program from Top to Bottom: One and a Half Day In-Person Seminar

Course Description:

Companies face many common issues and confusion when creating or revamping their validation programs. Some of them include:

• While an organization has ample experience in perfecting its process validation program, it may not be able to get its arms around the facility and equipment changes that require never ending equipment qualification (IQ, OQ, PQ).
• Customer or 483 audit findings require the company to deviate from its own validation program to meet the needs of the FDA or the customer.
• For systems that employ software and hardware, how does the company manage the validation activities, i.e. through the software validation effort or through the equipment qualification program?

The answers to these and many more typical questions and scenarios will be detailed in this training session designed to help manufacturers of FDA regulated products build (or rebuild) a sustainable validation program.

Note: Use coupon code 232082 and get 10% off on registration.

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