Organization: Health Canada
Year: 2021
Month: June
Request Number: A-2021-000303
Request Summary: For each COVID-19 vaccine that has been and/or is currently being administered in Canada under "emergency" authorization from Health Canada: the consent form(s) used to inform clinical trial participants of the potential risks and benefits of participating in the trial prior to enrolment, and/or to record whether informed consent was granted by a participant; the consent form(s) used to inform "COVID-19 vaccine" recipients of the risks and benefits of the "vaccine" prior to administration of such, and/or to record whether informed consent was granted by a recipient; all additional records that show or explain or reveal: The information provided to participants/recipients prior to enrolment/administration, and/or the metholodgy(ies) used to obtain and record informed consent from participants/recipients; records demonstrating whether the Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans: TCPS 2 (2018) Chapter 3 the Consent Process is adhered to in Canada; all records that show or explain or reveal: What follow-up information is collected for each participant/recipient in order to track their response to the "COVID-19 vaccine" (or placebo), and/or the metholodgy(ies) used to obtain and record said information; all records that show or explain or reveal how the outcomes for "COVID-19 vaccine" recipients in Canada are being monitored and recorded, on both an individual and population level.
Disposition: No records exist
Number of pages: 0