About Us

MMS is a quality focused CRO supporting the top 10 big pharma as well as multiple smaller companies 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 over two decades of hands-on drug development experience that helps support program-level strategy and execution of projects across multiple therapeutic areas. Continual staff training, innovative recruitment and motivating career options 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 is configured 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 the client.

Regulatory Submission Support Based on Strong Science and Strength of Process. We Do Data Best!

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