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:
- Protocol and results registration on ClinicalTrials.gov, EudraCT, and other global registries
- Full workflow management
- Provision of summary writers and QC analysts for overall workflow management
- Ability to integrate with your systems to help leverage existing data, gain efficiencies, and improve reporting accuracy
State of the Art Technology
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.