Electronic Archives for Regulatory Retention Compliance in Life Science Industries and Clinical Trial Research

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