Research Services 

The CNS provides expert consulting services to support your research at any stage.

Our Clinical Research Services

Study Planning

  • Literature review
  • Sample size analysis
  • Study design
  • Protocol development based on ICH guidelines
  • Templated protocols:  Adaptable study design to facilitate modifications for use across multiple studies or interventions
  • Study summary document to generate interest from funders and stakeholders
  • Informed Consent Form development
  • Focus Groups for patient-oriented research

Operational Support

  • Good Clinical Practice (GCP) training   
  • Customized Case Report Form (CRF) development  
  • International shipping coordination and support   
  • Vendor management  
  • Study-specific recruitment and marketing (graphic design, website, social media, video production, google ads)  

Study Submissions

  • Institutional or Central Research Ethics Board
  • Health Canada ITA & CTA application support
  • Section 56 exemption applications for controlled substance use in research

Post-Study Communications

  • Statistical analysis and reporting  
  • Manuscript writing and submission to peer reviewed journals  
  • White papers  
  • Press releases  
  • Grant writing  
  • Knowledge translation activities (e.g. infographics, videos, conference presentations)