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What Envision Research Can Provide To Your Clinical Trial Site

• Connect your practice with leading pharmaceutical, and medical device sponsors and Contract Research Organizations (CRO)
• Feasibility assessment
• Contracting and budgeting
• Regulatory and Institutional Review Board (IRB) management
• Study-specific site training
• Infrastructure and resources needed to conduct clinical trials, including support by experienced clinical research coordinators
• Standard Operating Procedures (SOP) for quality assurance
  Patient recruitment strategy
• Data management
• Clinical Trials Management System (CTMS)
• Adherence to Good Clinical Practice (GCP) and quality control
• Timely and successful completion of clinical trials