Automating your quality management system can transform your path to compliance with FDA, ISO, and GxP. This white paper explores the benefits of a centralized QMS, common pitfalls, and best practices when transitioning to eQMS.
When it’s time to start, or continue, leveraging software technology for automating your quality management system (QMS) processes there are key steps and major mistakes to avoid to ensure you set your system up for long-term success. Whether you have one or more electronic quality processes in place that you want to improve, or you’re looking to implement automation for the first time, this white paper with companion checklist offers:
- Essential steps and pitfalls when planning and implementing an automated QMS
- Explore common real scenarios where projects fail
- Outline key strategies for long term success with your automation project