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Clinical Trial Operations

Home Clinical Data Management

MFPL has experience Clinical Operations Team which is built to deliver fast, efficient investigator site support and data oversight for your study. MFPL has partnered with some of the largest pharmaceutical, biotech and device companies, providing innovative and customized clinical trial and research services.

We have successfully completed Phase 1, 2 and 3 trials utilizing high quality protocols and Good Clinical Practices (GCP). Our services are efficient in implementing complete clinical trial management, medical monitoring, data management and site management services including risk-based monitoring all from start to end, to ensure that all aspects of the trial are professionally

handled with quality and integrity of data in order to establish the shortest route to market for our client’s product. Our risk-based monitoring enables us to provide our clients with various options in executing FDA or applicable regulatory guidances.

MFPL provides expert services in all key areas of the Clinical operations process including:

  • Selection of sites and Feasibility Assessment
  • IP Management
  • Translation services for clinical trial documents
  • Vendor Management
  • Clinical trial monitoring, Medical monitoring, Supervision and Quality control of equipment and processes, etc.