Clinical Trial Disclosures

The MMS Disclosure Services team is your ideal strategic outsourcing partner for clinical trial disclosures. Our Staff Expertise, Proven Processes, and Exclusive Technology (TrialAssure) ensures quality of data, regulatory compliance, completeness of workflow information, providing comprehensive disclosure reporting all in a centralized, cost-effective manner!

Trial Assure Formula

Staff Expertise

MMS employs industry professionals who have managed disclosures for some of the largest pharmaceutical companies. Our subject matter experts have been involved with disclosures for over a decade with a solid understanding of the evolving regulations.

Proven Process

  • Managing the workflow through a proven and proprietary 10+ step process for US and international registries
  • Summarizing information with proprietary checks and balances to meet both internal and external requirements

Full Service Workflow Operations

Through our Integrated Disclosure Solution (IDS), this service allows MMS to be your centralized disclosure department and manage all Workflow and (optional) Data Summarization obligations for an entire drug development pipeline. Simple, periodic inputs from the trial sponsor allows MMS to manage the 10-step workflow including tracking, assessments, document management, summarization, review cycle, quality checks, approval cycle, release information to registries, registry query cycles, and monthly site/status updates for US and international registries.

Workflow Augmentation

Your staffing may have the capability to manage most disclosure workflow steps in-house, however, could use strategic augmentation.  Let MMS seamlessly integrate into your organization with the following service offerings:

Summary Writers

Provide us your source documents, and our experienced Disclosure Summary Writers can summarize your data into the required content and format for ClinicalTrials.gov, EudraCT, or any of the other 15 mandatory international registries.

Quality Control Analysts

Let your in-house clinical or medical writing staff summarize your disclosures, but have our QC Team experienced in the content and format of disclosures conduct a quality review of each summary prior to release.

Call Center

Sponsors of clinical trials are required to enter Central Contact or Facility Site Contact Information for each active study posted on ClinicalTrials.gov. MMS serves as a central contact and our call center staff effectively guides callers to a facility in their local areas.

Exclusive Technology

TrialAssureTM is a proprietary software reporting tool that summarizes your data and facilitates workflow. It ensures quality, compliance, and completeness of clinical disclosure reporting, while serving as a centralized and definitive (single source) catalogue across an organization’s drug development pipeline.

Built by Industry Professionals for Industry Professionals

Through our Integrated Disclosure Solution (IDS), this service allows MMS to be your centralized disclosure department and manage all Workflow and (optional) Data Summarization obligations for an entire drug development pipeline. Simple, periodic inputs from the trial sponsor allows MMS to manage the 10-step workflow including tracking, assessments, document management, summarization, review cycle, quality checks, approval cycle, release information to registries, registry query cycles, and monthly site/status updates for US and international registries.

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

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