Canadian Centre for Clinical Trials’ experienced research staff will design individualized clinical trial protocols optimized to meet study outcomes. The protocol will provide a detailed explanation of the clinical trial to be conducted, including the study’s aim, methodology pertaining to data collection, outcome measures, data analysis and conclusions. All protocols are written in abidance with the Good Clinical Practice (GCP) guidelines.
Study Templates Design
The qualified research team at the Canadian Centre for Clinical Trials can design all necessary source documents for accurate data capture as outlined in the protocol.
This includes but is not limited to:
- Informed Consent Forms (ICF)
- Case Report Forms (CRF)
- Assessment Schedules
- Investigator Brochures