Document Workshops

MasterControl's On-site Document Workshop Teaches Participants How to Document a GMP/ISO-Compliant Quality Management System (QMS)

Regardless of sector, size, structure, or maturity, regulated organizations must establish an appropriate quality management system (QMS) to be successful. The most important aspect of any QMS is the way in which it is documented to manifest the system hierarchy. The two-day document workshop, delivered on-site at the customer's facility of choice, explores the process model approach for the creation and operation of an effectively documented QMS - one that complies with FDA, ISO, and other regulatory standards. The levels of complexity, integration, and application are examined to bring about a streamlined system that is effective, efficient, and not burdened by superfluous documentation.

MasterControl QMS Overview
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