The archiving of regulatory content is a focus for global regulators and a major challenge across the Pharma/Biotech Industry. Vast amounts of data, records and documents are generated for every new product and the transition to electronic archiving via an EDMS will allow organisations to successfully operate a reference library for long term retention and retrieval of electronic documents.
Listen to this webinar with a panel of experts to learn how to build towards and manage e-archiving in compliance with regulatory mandates and industry best practices.
- Archiving Industry Expert – Dr. Teri Stokes, Ph.D., Director GXP International
- Practicing Archivist – Dave Ives, Assoc Director, Regulatory Operations, Vertex Pharma
- Archiving Solution Demo – Murtuza Vasowalla, BIOVIA, Director, Global Solutions Consulting
Duration: 65 mins