Quality assurance is important in every sector, especially in the pharmaceutical sector where complete documentation of data modifications and production and quality control data are carefully monitored. In addition, a wide range of legal standards and GMP guidelines (FDA, FMD, EMA, BRC, IFRA, GHS etc.) must be respected.

The document management system for this sector must therefore be able to be tailored to the standards and legislation in force, including the audit trail for all documents.

These companies in the pharma sector use Smartdoc.