The Research Compliance and Training team is dedicated to fostering a culture of compliance in human participant research. The team aims to promote quality, streamline processes, improve efficiency, and minimize risks of harm.
Compliance and Training resources and supports for all types of human participant research can be found under one of the streams below:
For questions or additional information, please reach out to the Compliance and Training Team.
including newsletters, notifications of upcoming events and more.
A variety of instructional resources are available to help members of the Queen’s Research Community confidently engage in ethical and compliant research involving human participants.
For questions, additional information, or a missing topic, please reach out to the Compliance and Training Team.
MANDATORY
| Applicable to | What | Time | How |
|---|---|---|---|
| All Queen’s University and affiliated hospital researchers and research team members conducting research involving human participants, including their data and/or biological materials. | TCPS 2: CORE-2022 Tutorial | 2.5-4 hours | |
| All researchers and research team members involved in clinical trials |
Good Clinical Practice (GCP) | 3-4 hours | /vpr/ethics/citi |
| Plus applicable regulatory training: | |||
| Drugs - Health Canada Division 5 (food and drug regulations, Part C, division 5 | 3-4 hours | /vpr/ethics/citi | |
| Natural Health Products - PART 4 - Clinical Trials Involving Human Subjects | 1-2 hours | Self-directed |
|
| Medical Devices - PART 3 - Medical Devices for Investigational Testing Involving Human Subjects | 1-2 hours | Self-directed |
|
RECOMMENDED
| Applicable to | What | How |
|---|---|---|
| An introductory course on Privacy and Security for Personal Information (PI) and Personal Health Information (PHI) in the research environment. | Foundations in Privacy in research. | /vpr/ethics/privacyinresearch |
| Recommended for all researchers regardless of discipline or career stage. | Responsible Conduct of Research (RCR): This module introduces concepts and principles related to what has come to be known as the Responsible Conduct of Research (RCR). | /vpr/ethics/citi |
|
Biomedical Research: an introduction to a variety of ethical issues that are important to consider when conducting biomedical research with human participants not limited to clinical trials. For more advanced users, the Tutorial is an educational tool that will assist in the understanding and appropriate application of ethical principles, guidelines, regulations and legislation when conducting biomedical research. |
|
| Intended for CRCs, investigators, and other clinical research professionals; intended as foundational role-based training for learners needing basic CRC training or organizations needing on-boarding training for new CRCs. | Clinical Research Coordinator |
Supporting the compliant conduct of human participant research by providing:
- Standard operating Procedures for Clinical Research
- Tools and templates
- Clinical Trial Registration
For questions or additional information, please reach out to the Compliance and Training Team.
Standard Operating Procedures for Clinical Research:
¾ÅÐãÖ±²¥ is a member of the Network of Networks (N2) and provides affiliated researchers with access to N2’s complete set of Clinical Research Standard Operating Procedures (SOPs) and clinical research templates. These SOPs are compliant with TCPS2, ICH-GCP and both HC and US FDA regulations for clinical research.
Use of these SOPs for clinical research is highly recommended by the Compliance and Training team. For affiliated hospital-based research, please consult with the KGHRI and PCC research teams for requirements. If used, training is required and must be documented; a Training log is provided below.
Other SOPs Resources
| Document | Category |
| Rollout Material | |
| N2 V10 SOP Quiz with Justification (May 2023) | Rollout Material |
| N2 V10 SOP Quiz without Justification (May 2023) | Rollout Material |
| N2 V10 SOP Rollout Letter (May 31, 2023) | Rollout Material |
| Table of Contents | SOP Table of Contents |
| Training Log | Training Log |
| Glossary of Terms | Glossary |
Tools and Templates for Clinical Research
The Compliance and Training team is currently developing resources for Investigator-initiated clinical trials but through our membership in the Network of Networks (N2), we have access to N2’s complete set of Clinical Research tools and templates. Didn’t find what you are looking for? please reach out to the Compliance and Training Team.
Didn't find what you were looking for?
Clinical Trial Registration
Clinical trial registration helps to promote transparency in research, prevent publication bias, and reduce duplication of efforts. Registration in a publicly accessible registry that is acceptable to World Health Organization (WHO) or the International Committee of Medical Journal Editors (ICMJE). is required before recruitment prior to the first participant visit per TCPS2 and NIH policies.
Registration is completed by the sponsor or sponsor-investigator for investigator-initiated research.
The registry that is used by ¾ÅÐãÖ±²¥ and its affiliated hospitals (KHSC and PCC) is
For assistance with this process, please contact the Compliance and Training Team, or the research teams at the affiliated hospitals (kghri@kingstonhsc.ca, research@providencecare.ca)
Once registered, the registry must be maintained and updated in a timely manner as follows:
- records must be reviewed and verified at least once every 12 months. For ongoing studies, it is recommended that this be done every 6 months.
- In a timely manner (15 or 30 days) with:
- new information that might affect the welfare or consent of participants,
- safety and efficacy reports,
- reasons for stopping a trial early
- the location of findings
- Individual site status and overall recruitment status (within 30 days of the change)
- Primary completion date (within 30 days of the change)
For CIHR-funded clinical trials:
If you have received CIHR GRANT FUNDS FOR CLINICAL TRIAL RESEARCH AFTER JANUARY 1, 2022, you must additionally ensure:
- All study publications include the registration number/trial ID
- Publications describing clinical trial results must be open access from the date of publication.
- Summary results must be publicly available within 12 months from the last visit of the last participant (for collection of data on the primary outcome). This is congruent with NIH funding policy, as well as the .
For more information, visit CIHR page
The Compliance Team is available to guide you through the ethical and compliant conduct of human participant research throughout the life cycle of your research project - from concept through to study closeout and publication.
We offer expert guidance and consultations for all types of studies that involve human participants, from anonymous surveys to interventional new drug clinical trials.
Please reach out to the Compliance and Training Team.
The Compliance Team provides oversight of human participant research. We handle reports of alleged non-compliance and work closely with the Research Ethics Office and the research teams at the affiliated hospitals. While the human participants protection program is currently under development, we are pleased to offer various oversight services including compliance readiness reviews and inspection preparation.
Please reach out to the Compliance and Training Team.
Weekly virtual drop-in session
The Compliance and Training team are hosting weekly virtual drop-in sessions every Tuesday between 10 - 11 am.
The aim is to support our research community the ethical and compliant conduct of human participant research throughout the life cycle of a research project - from concept through to study closeout and publication. If we cannot answer your question in 5 minutes, we will arrange a separate meeting to help you navigate.
Ashley Theis
Associate Director, Research Compliance and Training
355 King St. West