Regulated and standards-certified companies that are still reliant on paper-based and decentralized electronic processes are facing rough waters ahead. The Coronavirus pandemic and disruptions across the global supply chain have contributed toward an even stronger push for automating quality management systems (QMS).
A fast-changing business environment requires rapid access to intelligence. The pandemic demonstrated how fast operations can change, and exposed the susceptibility of poor quality management practices.
This guide discusses the importance of an automated enterprise quality management system (EQMS) for medical device and diagnostics, pharmaceutical, biotechnology, and other manufacturing companies. It identifies common pitfalls that can impact different phases of a QMS project implementation, as well as recommend actionable strategies for overcoming them.
Learn More About:
- Market and regulatory forces that make a QMS essential in today’s manufacturing industries
- Business benefits of an integrated, digital QMS
- Common practices that can derail a QMS upgrade
- Proven industry best practices for a successful QMS implementation and future improvements