Pre-Market, Clinical Trials, & Post-Approval Projects

Reduce time, save money

M2S delivers experience, a true understanding of the product development process, and expertise in project management and registry development to transform real world registry data into valuable information for industry solutions. Working with society members, medical device partners and regulators, we provide data that leads to a better understanding of the benefits and risks of existing and new devices. Our PATHWAYS Clinical Platform gives you tremendous flexibility to design new studies, or provide robust mining and tailoring of existing data.

BETTER ON EVERY LEVEL

M2S has the answer. We offer:

  • Dedicated project management throughout the life-cycle of your project.
  • Alignment with FDA initiative to use registries to collect real world data for post approval surveillance.
  • Real world data to verify a product’s risk-benefit profile and determine  long-term effectiveness.
  • An existing network of nearly 500 potential centers and 3,000 specialists experienced in data collection.
  • Simplified data collection, using existing registry platform, while having  the option to add project-specific custom content.

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VQI/INDUSTRY PROJECTS

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