ISO 9001:2015   |   ISO 27001:2013

About Us

MMS is a quality focused, global CRO that supports leading pharmaceutical and biotech companies as well as many smaller enterprises across our spectrum of services. Having completed more than 50 submissions for drug approval over the last 5 years, we remain a top choice for sponsors who are looking for innovation and demand high quality from their CRO partners.

Senior leadership at MMS has more than two decades of hands-on drug development experience which helps support program-level strategy and execution of projects across multiple therapeutic areas. Continual staff training, innovative recruitment and motivating career opportunities help MMS retain the best talent and develop a strong, client-focused workforce across all global locations.

Adaptive Parallel Processing™

For each project we undertake, the internal MMS team collaborates using Adaptive Parallel Processing™, a unique, trademarked system that allows flexibility, subject matter expertise, process optimization and risk planning for the project to ensure on-time delivery and added value to each client.

Regulatory Submission Support Based on Strong Science and Strength of Process. The difference is in the data!