Regulated Clinical Development for the U.S. and International Regulatory Agencies

MQI implements all aspects of a clinical trial.

• Project management
• Protocol development
• Investigative site selection
• Institutional Review Board (IRB) submissions
• Clinical study initiation and monitoring
• Medical monitoring & study site compliance
• Clinical data management and data analysis
• Statistical plan development and analysis
• Regulatory submission

Throughout the clinical study, and at all times during product development, we focus on the end point of regulatory approval of your product and commercialization.