Our Services

Health Canada REB submissions CRC and GCP Ontario, Alberta, Manitoba

How a study runs

  1. Before

    Getting approved

    • Study design
    • Regulatory documentation
    • Site agreements
    • REB submission

  2. During

    Running the study

    • Site preparation
    • Enrollment
    • Data and specimen collection
    • Monitoring

  3. After

    Handing it back

    • Data cleaning
    • Chain of custody
    • Statistical analysis
    • Reporting

Discuss a study

Send the protocol and the sites you have in mind. We will come back on feasibility, timelines and what we can cover.

Contact us