The European Union’s General Data Protection Regulation requires every organization that collects sensitive personal data from those residing in the EU to ask for clear and specific consent ...

The plan for obtaining consent must be included in the Human Subjects Protocol. Investigators may request a waiver or alteration of the informed consent process or waiver of consent documentation, ...

Use short paragraphs, bullets and subheadings to increase readability. See the informed consent form template (pdf) for more help and sample language. 1. Title of the Study 2. Names and Affiliations ...

The Revised Common Rule requires all clinical trials to post an unsigned consent form on a publicly available website ... is to increase transparency for federally funded clinical trials and ...

There is no need to utilize the UAB IRB’s Sample Consent form for consent processes in exempt research. Your consent process should be clear and contain full sentences that are in no more than 8th ...

Investigators should follow the required elements of informed consent when preparing a Parental Consent Form, except that the form is written for the parents so ... status, and condition. This sample ...