PARTNERSHIP ANNOUNCEMENT

Greenlight Guru and VISDOM bring medical device solutions that accelerate the delivery of life-changing devices. Greenlight Guru’s Medical Device Success Platform coincides with VISDOM's ability to provide the seamless transition from in-house records management to MDR and FDA compliance.

Customers benefit from leading eQMS and full service managed GRC, MDR and QMS provider for medical device companies

Greenlight Guru and VISDOM both have the same goal and mission: To improve the quality of life by helping medical device companies and manufacturers get to market faster with less risk. The problem? Medical device companies were forced to leverage outdated, industry agnostic, inefficient tools and resources.

Greenlight Guru created the only Medical Device Success Platform (MDSP) in the industry, focused on quality, regulatory, and product development. With Greenlight Guru, there is a single source of truth accessible by both product and quality teams that streamlines collaboration and compliance, without stifling product development efforts.

On the same mission, VISDOM has tackled the difficulties of navigating the regulatory pathways. VISDOM provides a one-stop-shop of resources and tools to help medical device companies become EU MDR compliant and guidance on help obtaining ISO 13485 certification.

Both Greenlight Guru and VISDOM are disrupting an industry to provide tools and resources built for the medical device industry.