Greenlight Guru and Lexisnexis® Reed Tech Announce Strategic Alliance to Guide Customers to Market Faster

February 24, 2022

Greenlight Guru has teamed up with LexisNexis® Reed Tech, the leader in regulatory product data submissions to global health authorities

Reed Tech Partnership graphic

INDIANAPOLIS — February 24, 2022 — In response to the needs expressed by medical device manufacturers for ways to effectively manage the product lifecycle from conception through regulatory clearance and post-market activities, Reed Tech, a leading provider of data management and analytics solutions for the life sciences industry, is building an alliance of world-class solution providers, a collective of regulatory experts delivering solutions and services who support manufacturers, distributors and related operations. Answering the call for innovation in quality management systems, Reed Tech has expanded its collaboration with Greenlight Guru, the pioneer of the only dedicated Medical Device Success Platform (MDSP), serving the specialized workflows of manufacturers. Current and prospective customers of both companies can leverage exclusive benefits as part of this new strategic alliance.

“Greenlight Guru is pleased to have an industry-leading UDI submission answer to solve for this step in the regulatory process. Reed Tech is a core UDI submission provider for many manufacturers around the world, large and small. Our customers can benefit from their specialized understanding of regulatory submission requirements for medical device manufacturers,” said David DeRam, CEO of Greenlight Guru. Manufacturers bringing new products to market or maintaining existing portfolios will benefit from the subject-matter expertise offered by Reed Tech.”

 “Implementation of Unique Device Identification (UDI) product data within US FDA, EU EUDAMED, China NMPA, South Korea MFDS, and other health authority databases creates complexity for medical device manufacturers. Reed Tech SingleSource™ for Medical Devices, along with the quality management and regulatory expertise of Greenlight Guru helps manufacturers in implementing best practices. With world-class workflow solutions, QA/RA professionals around the world benefit from superior, end-to-end traceability and quality standards to streamline efficiency, reduce risk and meet the compliance requirements of local health authorities,” said Arshad Rahman, General Manager of the Reed Tech Life Sciences division.

Medical device manufacturers and labelers are continually upgrading processes and preparing for multiple global health authority requirements. The complementary solutions and services between Greenlight Guru and Reed Tech offer critical efficiency gains in managing the product life cycle.

Learn more about our strategic alliance by visiting

Nick Tippmann is an experienced marketing professional lauded by colleagues, peers, and medical device professionals alike for his strategic contributions to Greenlight Guru from the time of the company’s inception. Previous to Greenlight Guru, he co-founded and led a media and event production company that was later...

Search Results for:
    Load More Results