CCS Services

The vision of CCS is to provide drug and device sponsors with unparalleled clinical development and clinical trial management services that are academically informed and clinically focused on cardiovascular research.

CCS provides the following services:

• Clinical Development Strategic Consultation
• Protocol Development
• Informed Consent Development
• Trial Budget Preparation
• Centralized Site Selection
• Centralized Site Contracting
• Central Regulatory Document Collection & Review
• Central IRB Approval
• Clinical Economic Analysis
• Investigator Meeting Management/Academic Support
• Site Management
• Site Monitoring
• Data Management
• Data Interpretation/Presentation/Publication
• Medical Monitoring/Clinical Help Line
• Safety Reporting
• Cardiac nurse-staffed Call Center
• Cardiovascular Event Adjudication
• Executive Committee Management (Clinical End Point Adjudication Committee/CEC, DSMB, Steering Committee, Advisory Board)
• Cardiovascular Imaging Core Laboratory Services
• Cardiovascular End Point and Quality of Life Assessments
• Pharmacoeconomic studies