At the National Prion Clinic we may ask our patients and research participants for consent to take a blood sample. These blood samples are used in studies investigating causes of and possible ...

The consent process is fully discussed in Chapter 3 of the Tri-Council Policy Statement Ethical Conduct for Research Involving Humans (TCPS 2). This includes a discussion of the information generally ...

These guidelines and sample consent form are intended for researchers who need assistance in creating a Consent Form for research involving human participants. If you have questions about your form or ...

The sample consent forms are being provided to you as a tool. They contain all of the required elements of an acceptable consent form. While we strongly recommend that you follow the format that we ...

Below are sample documents and forms that can be used in the immunization process for your reference. These sample documents are not intended to be filled out and sent to the Public Health Agency of ...

All new studies approved by the IRB on or after January 21, 2019 must comply with the Revised Common Rule. One change included in the Revised Common Rule is a new requirement to post an informed ...

Ethicists have suggested that written consent forms encourage participants in phase 1 cancer trials to expect benefit from the experimental agent and to overlook serious risks. Of 272 forms, 268 ...