Survey Finds 81% of Medical Device Companies are Not Using Tools Designed for the Medical Device Industry in Their Quality Management Processes
Summary
“To find that more than 80 percent of organizations are asking their quality and engineering teams to ‘make do’ with legacy tools and solutions is as an eye-opener,” said David DeRam, CEO of Greenlight Guru. Survey respondents consisted of 524 participants, 93 percent of whom represented quality, regulatory, engineering and operations professionals from small and enterprise-size device makers. To download the full 2020 State of Medical Device Product Development & Quality Management, please visit https://www.greenlight.guru/state-of-medical-device. The platform helps companies bring safer products to market faster, simplifies FDA and ISO regulatory compliance and provides a single source of truth by connecting the management of all quality processes like CAPAs, risk, audits and more. Greenlight Guru’s platform is used by thousands of users across the globe to push beyond baseline compliance and achieve True Quality for their medical devices.
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