Greenlight Guru and PathWise Announces Joint Training Event in Switzerland
INDIANAPOLIS (PRWEB) May 01, 2018 -- Greenlight Guru, the only cloud-based quality management software specifically for medical device companies, is pleased to announce a new strategic partnership with PathWise, a Utah-based training and consulting firm that works with medical device, pharmaceutical and biotechnology companies in the areas of quality and compliance.
“PathWise is well respected in the medical device, pharmaceutical and biotech regulatory consulting and training industry,” says Greenlight Guru co-founder and CEO David DeRam. “This partnership will allow us to combine our purpose built quality management software platform with PathWise’s on-site training curriculum to serve a quickly developing market.”
The relationship will consist of on-site training to provide education and guidance on the rapidly evolving domestic European Union medical device regulatory environments, including MDR 2017/745 and the coming MDR 2020 implementation deadline. The training will be hosted in Basel, Switzerland June 27-29.
“We are excited for this joint venture with Greenlight Guru to help meet the needs of our clients on a domestic and international scale,” says PathWise President and CEO Nate Conover. “It’s not only mutually beneficial for us as individual organizations, but it will benefit our customers in a big way. This teaming brings together the hands-on experience and quality system process understanding PathWise is known for with cutting edge technology of the Greenlight Guru eQMS, in order to give our event participants everything that they need to be ready and compliant in general for their organization, and specifically for when the MDR 2017/745 goes into effect.”
Training programs are appropriate for design engineers, quality assurance and regulatory compliance personnel. Registration for the May 3 webinar and the June 27-29 training courses in Basel, Switzerland are now open.
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.
About PathWise
In a globally regulated life science industry, PathWise provides proven methodologies in quality and compliance through best in class training that ensures compliant, effective, and efficient quality systems. Since 1993 PathWise has worked with the best in the life science manufacturing industries and brings an intimate knowledge of regulatory and compliance standards to move your organization forward in quality and compliance. For more information, visit http://www.pathwise.com.
Nick Tippmann, Greenlight Guru, https://www.greenlight.guru/, +1 (260) 438-8708, [email protected]
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