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INDIANAPOLIS (PRWEB) October 30, 2017
Greenlight Guru announces the addition of Grow to its existing quality management software platform, helps companies get high quality medical devices to market faster and with less risk. Now, with the introduction of their Grow product, Greenlight Guru’s software can assist medical device companies after the launch of a device by connecting its entire quality ecosystem and advancing the success of high-quality devices already on the market.
According to the FDA, Corrective and Preventive Actions (CAPA) continue to be the number one reason medical device companies are cited for 483 Observations. The reason is because many medical device companies are still using a paper-based system to connect the disparate processes, sources, people and data within a quality system. Or, the companies are opting for an eQMS that isn’t tailored toward the medical device industry and doesn’t address the changing FDA regulations and ISO standards in which the medical device industry must adhere.
“After experiencing this pain firsthand working in product development and management for medical device companies, I knew there needed to be an easier way to help companies not only get to market faster but improve their postmarket quality processes beyond just compliance,” said Jon Speer, founder and VP of QA/RA at Greenlight Guru. “Grow has additional workflows for CAPA and other postmarket needs that will help these companies who are flying blind without visibility into their quality system and are subject to unnecessary risk."
With Go, Greenlight Guru’s first product, companies utilize design control, risk management and document management software to bring FDA and ISO-compliant medical devices to market in less time. Now with Grow, companies will have the necessary visibility into all their quality processes to achieve True Quality by applying:
"The new Greenlight Guru Grow product will be very helpful in our ability to escalate and manage quality events that require a CAPA investigation,” said Eric Rock, customer and QA/RA Manager, Litecure. “Being able to easily link and connect nonconformances, complaints, audit findings, CAPAs and documents will greatly improve our internal efficiency and compliance and allow us to put our focus squarely on the quality of our products."
"Grow is a disruptor for the medical device industry," said David DeRam, co-founder and CEO at Greenlight Guru. "Companies can now use quality as an accelerator, confidently connecting all the pieces of their quality system to get the visibility they've been missing, leading to higher quality devices, better business and ultimately, better lives.”
To learn how to implement and maintain a modern CAPA system while avoiding the common pitfalls, register for Greenlight Guru’s upcoming educational webinar with FDA News on November 8, 2017.
For more information or to get a demonstration of the new Grow product please visit http://www.greenlight.guru.
About Greenlight Guru
Greenlight Guru is the only quality management platform designed specifically for medical devices companies. The platform helps companies get 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 achieving True Quality. For more information, visit http://www.greenlight.guru.
BLASTmedia for Greenlight Guru
office: 317-806-1900 ext.142
For the original version on PRWeb visit: http://www.prweb.com/releases/2017/10/prweb14855470.htmNEXT ARTICLE
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