Informed consent for research participation is a fundamental part of protecting human research subjects. This idea is at the core of one of the Belmont Report’s ethical principles, respect for persons ...
Informed Consent and HIPAA Authorization Form Template v24AUG2026: This template should be used as the consent document guide for all new research studies, including parental and LAR permission ...
Enhancing Goal-Concordant Care in Oncology: Development and Impact of an Institutional Communication Skills Training Program Approximately 8% of the US population speaks primary languages other than ...
The US Food and Drug Administration has issued warning letters to several drug makers for failing to meet its current good manufacturing practices (CGMP) requirements and a company for failing to ...
An informed consent form is the written document a participant reads and signs (or that documents an oral consent process) before enrolling in research. Regulations tell institutions what the consent ...
Researchers working with human subjects are required to submit their studies for review and approval by the Institutional Review Board (IRB). To streamline this process, our institution transitioned ...
A new harmonised template (Version 2.0) for participant recruitment and informed consent is now available for all clinical trials conducted in the EU/EEA. The template has been developed by the ...
The forms and templates found below are intended to be useful tools for you as you prepare for and implement your research project. Information Sheet Templates (Updated September 2026) These templates ...
Failure to obtain informed consent can result in significant consequences Exceptions to informed consent apply only in limited circumstances Elements of valid informed consent include patient capacity ...
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