Clinical Trial Management

MPACT understands that a successful clinical trial can only be completed through the expertise of Principal Investigators. These are physicians who are interested in being at the cutting edge of medicine and apply their vast clinical knowledge to advance drug development.

A physician in the network benefits from the many centralized services offered by MPACT. These services include: marketing, budget negotiation and contract finalization, consistent feasibility questionnaires for new projects, turnkey operation for new sites, site development, patient recruitment and assistance in investigator led trials from study design to completion.

• Protocol training
• SOP training
• IEC submission
• ADR reporting
• Standard Operating Procedure development/revision
• Informed consent
• Strategies to enhance patient recruitment and retention
• Audit query resolution
• Safety documentation
• Assisting in site budget preparation
• Coordinating with CRO for site payments
• Data archival at site
• Internal Monitoring by qualified clinical research consultant (once in 2 months or as and when required)
• Periodical consultancy visits (as and when required)
• Quality improvement of ongoing projects

• Trained CRCs
• Training of investigators
• Training of study team