Clinical Trial Management

Mission3 provides the following solutions for Clinical Trial Management:

The Mission3 Clinical Trial Master File Management solution is a pre-configured, hosted application, deployed from a fully validated data center. Whether you are a large or small organization and currently using a paper-based or electronic TMF approach, Mission3 can drive significant operational advantages to your organization, including:

• Decreased costs – rapid deployment; no hardware and minimal software and IT resources.
• Improved productivity – quick and easy access to TMF documentation and reduced time to assemble TMF.
• Improved compliance – centralized access to latest, approved TMF documentation and ability to respond efficiently and accurately to inquiries from health authorities.
• Improved control of documentation – consistent organization of TMF allows secure access to documents, including the ability to compile compound-specific documentation to support requests from business partners.

Mission3’s Project Management module integrates with electronic trial and content management systems, breaking down the barriers between clinical data and regulatory submissions repositories thus significantly improving efficiencies of your business processes as well the quality of overall program delivery.

Mission3 offers the following capabilities:

• Integration with IWR / IVR and other electronic trial systems using our Direct Connector technology, which can be adapted for your systems.
• Reporting of various trial management metrics across Intelligent Systems to enable your Program Managers to relate trials with overall program progress and accurately predict product availability.
• Aggregation of hundreds or thousands of CRFs and automating their addition to submissions.