Forms & Templates Sample IRB Forms 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 ...

Research by Johns Hopkins epidemiologists has confirmed what some have long suspected about consent forms required of clinical trial volunteers: They use language far too difficult for most people ...

Consent Form Templates The goal of the informed consent process is to ensure that the research subject is treated with respect and human dignity. The process does this by safeguarding and advocating ...

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 ...

IRBs commonly present investigators with readability standards and informed-consent text, in the form of templates and sample forms.

Certinal has announced the launch of its new Consent Form Management System (CFMS), offering hospitals a modern solution to ...

NOTE: Templates for the short form consent document and the English-language consent document (to be used for the “summary”) are available in the researcher library in IRBNet. Short Form Informed ...

In my workplace, we have the consent signed prior to anyone from the anesthesia department seeing the patient. Is this safe and ethical?