A new consent form template has been published and is available on the Forms & Templates page. Note that with this new template informed consent forms will no longer be stamped with an expiration date ...

The IRB Office published an updated version of the informed consent template. The template and instructions for uploading this form in eRA have been posted to the Forms & Templates page. For your ...

Templates & Types of Informed Consent Click on each header below to learn more about the various types of consents. Each type of consent has a template that can be used in each scenario. Note: The ...

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 ...

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

Informed consent forms for interventional oncology clinical trials are often lengthy and written at too high of a reading level for some patients, making it hard for them to weigh the decision to ...

Defines informed consent Outlines where to find the most up-to-date consent form template, the HRP-502 Identifies the parts of the Informed Consent form Shares how to deliver information to potential ...

Informed consent is one of the primary requirements of research involving human participants. It is important to remember that informed consent is an ongoing process, not a document or single event.

A cornerstone of the dental practice, as with most healthcare professions, is the requirement to obtain informed consent before commencing treatment and procedures. The ADA Code of Ethics provides ...

Clinical research sponsors, IRBs, research institutions, and clinical research service providers should review current informed consent form templates and related policies and procedures to ...