Greenlight Guru & bioaccess™ Collaborate for Faster LATAM Studies and Enhanced Patient Outcomes

Customers benefit from leading eQMS, EDC, and industry-dedicated contract research organization (CRO) in Latin America

[MIAMI, FL, May 3, 2022] – Greenlight Guru and bioaccess™ share the same goal and mission: To enhance the quality of life by helping Medtech manufacturers get to market faster, with less risk. Greenlight Guru and bioaccess™ announce their cooperation agreement to bring medical device companies closer to Latin America, conduct early-stage clinical trials, or sell their innovations.

Greenlight Guru has realized that Medtech companies use outdated, generic, inefficient tools. Greenlight Guru has created the only purpose-built platform to give medical technology companies an end-to-end software solution to bring life-changing products to patients. With Greenlight Guru, medical device manufacturers have a single source of truth empowering product and quality teams that streamlines collaboration and compliance without stifling product development efforts.

bioaccess™ tackled another industry challenge: Foreign Medtech companies struggle to find an investigator for their early-feasibility clinical studies in Latin America. These companies are unfamiliar with the region and lack in-house experts to help operationalize a successful clinical strategy to ensure long-term success in Latin America. Since 2010, bioaccess™ has provided clinical research consulting services to foreign medical device manufacturers looking to succeed in Latin America with their first-in-human clinical trials.

"Now with bioaccess™ as a partner, our customers will now have streamlined resources for bringing their innovations to Latin America: a vast untapped region full of opportunities for fast, cost-effective, and quality early-feasibility clinical research and a promising market for the commercialization of medical technologies," said David DeRam, CEO of Greenlight Guru.

Both Greenlight Guru and bioaccess™ are leading the industry in providing solutions built specifically for the Medtech industry. The partnership presents Medtech companies with industry-specific out-of-the-box software solutions to automate quality, regulatory, and product development, as well as industry-specific clinical research and market access solutions to ensure their long-term success in Latin America.

About Greenlight Guru

Greenlight Guru is the only purpose-built platform to give medical technology companies an end-to-end software solution to bring life-changing products to patients. The platform integrates cross-functional teams, processes, and data throughout the entire product lifecycle, giving visibility and traceability beyond compliance requirements to proactively overcome execution gaps and accelerate success. Thousands of Medtech professionals are using Greenlight Guru’s platform across the globe to push beyond baseline compliance and achieve True Quality for their medical devices. For more information, visit www.greenlight.guru.

About bioaccess™

bioaccess™ is a US-based contract research organization (CRO) that delivers a full spectrum of clinical and regulatory service offerings so that foreign medical device companies can have long-term success in Latin America. For more information, visit www.bioaccessla.com.


Media contact

bioaccess.™

Julio G. Martinez-Clark, +1 (954) 903-7210

Chief Executive Officer

jmclark@bioaccessla.com

 

Greenlight Guru

Naomi Gollmer (419) 518-0067

Content/PR Specialist

naomi.gollmer@greenlight.guru

Previous
Previous

Cook Medical Treats First Patient in First-In-Human Clinical Trial for Venous Valve

Next
Next

Spine Stabilization Technologies Taps bioaccess™ for PerQdisc™ Latin America Launch!