ComplianceQuest can help companies to effectively plan, monitor, and improve the transition to quality management software as well as the overall quality management
ISO 13485:2016 has become the new foundation for medical device QMS or quality management software. If you haven’t started your gap analysis using quality management software, the time to start that transition is now. It is critical for medical device manufacturers and suppliers to begin implementing quality management software standards of the revised ISO 13485:2016, as the allotted three-year changeover period may not provide adequate time for all organizations to transition.
