Applying for Grants from CIHR - Video Tutorials
Are you a researcher looking to apply for a CIHR grant? Watch our informative video tutorials that will help you better understand the process from start to finish.
Clinical Trials and Compliance - Video Tutorials
Navigate the Health Canada clinical trial process with ease! This three-part series covers everything from completing the HC 3011 form and securing Ethics approval to mastering compliance. Start your trial journey with confidence and clarity.
Embarking on a clinical trial can be daunting, but preparation is key. In Part 1 of our three-part series, we outline the crucial first steps for submitting your trial to Health Canada. Learn how to identify your trial sponsor, accurately complete the HC 3011 form, and obtain the necessary signatures to move forward confidently. This video provides a clear roadmap to ensure you start your submission process on the right foot.
Important Links for Your Clinical Trial Submission
- Guidance on Completing the HC 3011 Form and Submission Package
Visit Health Canada’s Guidance Page - Access the HC 3011 Form and Related Documents
Health Canada Forms and Resources - Register Your Clinical Trial with ClinicalTrials.gov
Clinical trial registration is required.
Learn How to Register
Make sure to explore these resources for a smooth and compliant clinical trial process!
Securing ethical clearance is a vital component of any clinical trial. Part 2 of our series dives into the process of obtaining Ethics or REB Approval while working on your HC 3011 form. We guide you through the necessary review requirements, key documentation, and strategies to align with Health Canada’s expectations. This segment ensures you are well-prepared to meet the ethical standards essential for your trial’s success.
Important Link for Research Ethics Board (REB) Applications
Before starting your application, ensure you’re applying to the correct REB by reviewing the criteria here:
McMaster Research Ethics Board Criteria
Save time by confirming your REB pathway upfront!
Maintaining compliance throughout your clinical trial is critical. In Part 3 of our series, we focus on the regulatory and compliance framework that underpins a successful Health Canada-regulated trial. From Good Clinical Practice guidelines to essential training requirements, this video equips you with the knowledge to navigate the complexities of clinical trial standards. Completing this final step prepares you for a smooth trial journey.
Mandatory Training for Clinical Trial Researchers
All clinical researchers, staff, and students involved in clinical trials must complete the required training outlined in the Harmonized Research Training Framework.
Good Clinical Practice Training Details
Ensure you’re fully trained to meet compliance standards!