Market globalization has drastically increased the potential for profit for medical device manufacturers but it has also intensified competition and the pressure to produce devices faster and at a lower cost. The situation is even more challenging in ISO and FDA environments where companies must contend with stringent regulatory standards.
Since the ultimate goal of every medical device company is to maintain enduring compliance for lasting market success MasterControl has prepared a white paper that offers practical suggestions for fixing and enhancing quality management systems. Topics covered in the white paper include the automation of quality processes and the utilization of training as a tool for continuous quality improvement.
This white paper, “Six Ways to Optimize Your Quality Management System and Ensure FDA Compliance,” discusses subjects such as:
Methods of simplifying the compliance environment
Integrating training into quality management
Improving quality management with effective analytics and reporting tools
Adopting lasting validation as a strategy for compliance