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  • 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
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    • Responsibilities and qualification of CMX Clinical Research Coordinator
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    • CMX Research Inc. Designed and Initiated Trials

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Regulatory Submission

Clinical trials require continuous regulatory correspondence.  CMX Research Inc. provides our clients with strategic guidance on the clinical development plan, handles preparation and submission of all required ethics (REB/IRB) and regulatory (FDA and Health Canada) submissions.  We prepare and submit 7-day and 15-day safety reports as well as annual reports.

We provide our network sites with standard operating procedures, offer quality control and assurance, GCP/Privacy training, regulatory reviews and regulatory consulting.

Our dedicated team is focused on producing the most comprehensive, and submission-ready clinical data to ensure compliance with Health Canada, FDA and other regulatory agency requirements.  This guarantees that every phase of a trial will not be delayed due to regulatory stumbles.