FDA Regulation

Seminar on Modern Approaches to Process Validation: Requirements for Process Design, Design of Facilities and the Qualification of Equipment and Utilities at Copenhagen, Denmark

Companies face many common issues and confusion when creating or revamping their validation programs. • Company has expertise in its process validation program but can never quite get is arms around the facility and equipment changes that require never ending equipment qualification (IQ, OQ, PQ),

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Date: 10 December 2015
Location: Hilton Copenhagen Airport, DK