GlobalCompliancePanel's seminar will provide an overview and in-depth snapshot of the process for managing V&V activities affecting product, process, equipment and the QMS. Company employees responsible for new product development, regulatory submissions, initiating/overseeing company-wide V&V planning should attend. The seminar will also cover design validation; sterilization validation; test method validation; software validation; process validation; design verification and process verification; DQ, IQ, OQ, PQ and other areas associated with the QMS.