• Home

• Company Overview
  • Our Company
  • Mission, Vision, Values
  • Management Team
  • Clinical Specialties
  • Client List

• Services
  • Full Service Clinical Research Organization
    • Project and Trial Management
    • Study Design & Protocol Development
    • Regulatory Submission
    • Site Monitoring
    • Safety and Medical Monitoring
    • Data Management and Statistics
  • Site Management Operations
    • Services for Industry
    • Services for Sites
  • Patient Recruitment Services
    • Centralized Advertising
    • Multiligual Live Call Centre
  • Clinical Research Coordination Services
    • Responsibilities and qualification of CMX Clinical Research Coordinator
  • Clinical Trial Consulting
    • CMX Research Inc. Designed and Initiated Trials

• CMX Client Login
  • Eligard Registry Login
  • CRC Login
  • BHOS Login

• Careers
  • Working for CMX
  • Career Opportunities

• News
  • Press Release

• Contact Us

Study Design, Protocol Development and Medical Communication

The scientific staff and medical writers at CMX Research Inc. work closely with our clients to develop and review study designs and protocols.  They will help to establish an optimal design that meets the research endpoints and objectives of a particular study in the most efficient way possible.  Our study modeling capabilities help to avoid costly errors in study design and subsequent delays.

The in-house medical writers of CMX Research Inc. are able to provide our clients with all study related documentation including study protocols, investigators brochures, informed consent forms, data presentations, final study reports, manuscripts, and other publication needs.