Protocol Development
SPIRIT Protocol

Informed Consent Forms
Assent Template 1
Assent Template 2 — Clinical Research
Adolescent Assent Template
Deferred Consent — Clinical Research (Resource)
Deferred Consent — Drug Trials (Resource)

Clinical Trial Application to Health Canada
CTA Application
Good Clinical Practice Guidance
ITA Application

Drug Development
Bay Area Research Logistics—Placebo Templates
Placebo Development

Quality Assurance and Clinical Monitoring
MICYRN is a member of N2 (Network of Networks) and has access to tools and resources for best practices in clinical research including Health Canada approved standard operating procedures. For more information regarding SOPs and ICH-GCP training certifications please contact us.

Patient Engagement
CIHR Patient Engagement Materials

Agreements
MICYRN Lawyer Network
Study Terms of Reference Checklist

CONSORT

The CONSORT - Transparent Reporting of Trials website provides a checklist to ensure proper trial reporting.

View checklist here

Biobanking Resources

View List Here 

Anything missing? Please contact us!