Over two decades helping clients navigate the difficult path of regulatory compliance.

In 2006, MMS was created by Dr. Uma Sharma, with a vision to turn a one-person consultancy into a global, data-focused CRO that caters to the unique and often changing needs of sponsors. Years later, with an industry-leading customer satisfaction rating, MMS stays true to its dependable and customer-driven nature. A science-first approach and strong processes have smoothed the waters for MMS clients resulting in positive organic growth year over year, with more than 950 colleagues worldwide.

MMS is a place where years of proven success have guided sponsors through their data services and regulatory submissions goals. When MMS takes on a project, colleagues become ingrained in that sponsor – taking on a greater level of care and guiding them towards a positive outcome.

Sponsors that demand high quality come to MMS for strong industry expertise, a scientific approach to drug development, and top talent. Sponsors stay with MMS for its flexibility, agility, and a “do what it takes” attitude that is unrivaled in the industry.

With a global footprint across four continents, MMS was proud to be named Best CRO – Specialist Provider in the Scrip Awards and Best Data-Focused CRO in the GHP Global Excellence Awards. In addition, MMS is certified as a Top Workplace in the United States and Michigan for two consecutive years as well as a Certified Great Place to Work in India.

Recently, the TOGETHER Trial, which uses an Electronic Data Capture (EDC) system designed, built, and maintained by MMS, won the Society for Clinical Trial’s annual Trial of the Year Award.

Our Values