MMS combines over a decade of staff expertise, proven processes, and an exclusive technology partner to achieve comprehensive clinical trial disclosures reporting for US, EMA, and other international registries. Our integrated disclosure solution allows MMS to be your centralized disclosure department and manage all workflow and data summarization obligations for an entire drug development pipeline.
Let MMS seamlessly integrate into your organization with the following service offerings:
Through our partnership with TrialAssure® we offer disclosure and transparency reporting software that summarizes your data and facilitates workflows in a comprehensive, cost-effective manner. To learn more about the TrialAssure® system, visit their website.
Regulatory Submission Support Based on Strong Science and Strength of Process. The difference is in the data!