Clinical Research Services
The CNS provides expert consulting services to support your research at any stage.
Our CRO 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)
