This on demand webinar will take approximately 1 hour to complete

Pharmaceutical and medical devices companies are frequently inspected by the authorities as a central element of supervision. Successfully completing a GMP regulatory inspection is critical to operations and commercial success of a company; this cannot be accomplished without proper preparation and management since proper inspection management techniques have to be used to mitigate the risk of receiving an observation for compliance gaps. This session will provide insight on understanding the most common regulatory agencies expectations and will discuss how to prepare for and manage the actual inspection and describe follow-up activities required for close-out, as well as real-life lessons learned through being involved and conducting audits.

 Continuing Education Credits are not available for this event.