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.
Download this white paper from Thought Leader and acknowledged industry expert Dr. Teri Stokes to learn about:
- System Backup Media VS. Electronic Archives
- Archive Principles and Archivist Responsibilities
- NASA’s Model for Archive Systems
- GAMP Good Practice Guide for Electronic Data Archiving