MRC professionals have managed all aspects of clinical trials from select services to the initiation, management and close out varied size and multi-country studies. We have the resources and expertise necessary to provide a broad array of services. Including:

• Project management for phase I –IV, post approval and registry studies
• Protocol writing services
• Coordinate and manage international multi-site trials
• Post marketing surveillance
• Study monitoring for devices, drugs, biologics and investigator-initiated studies
• Site identification and qualification
• Electronic case report form data capture
• Develop standard operating procedures templates
• GAP analysis
• Site initiation services and regulatory training
• Site development and management services
• Feasibility studies
• Data management
• Laboratory services
• Mock FDA inspections
• Quality control/quality assurance auditing
• Organize and manage team meetings (weekly/monthly) during Study, including contracting phase, to ensure early and ongoing communication and timely management of slow to respond sites and contract delays.