Moving forward, making informed consent truly informed – rooted in both equity and accessibility –  needs to be a priority, ...

Objectives: To study the consent process experienced by participants who are enrolled in a molecular genetic research study that aims to find new genetic mutations responsible for an apparently ...

A one-off paper-based consent form is not necessarily the best solution when it comes to obtaining consent from research participants for genome sequencing. A dynamic consent process that allows ...

Examples of limiters may be limiters imposed by the research consent, HIPAA requirements or any agreements with third parties about future use of the data. Additional JHURA Human-Derived Data FAQs are ...

This is a sample form, not intended for actual use. Please see the instructions for authors for the event at which your paper has been accepted for the appropriate consent form.

The traditional informed consent process involves written forms and obtaining signatures. This process remains the standard, but in various research settings, such as COVID-19 and rare disease ...

Background Genomic research is challenging the tradition of informed consent. Genomic researchers in the USA, Canada and parts of Europe are encouraged to use informed consent to address the prospect ...

Microsoft Research Project Participation Consent Form INTRODUCTION Thank you for deciding to volunteer in a Microsoft Corporation research project. You have no obligation to participate and you may ...

BENEFITS AND RISKS Benefits: The research team expects to collect videos of diverse signers from this project which we hope will improve the accuracy of sign language recognition systems for diverse ...

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 ...

The consent form templates and instructions address the requirements for informed consent and discontinuation of participation, including requirements to inform participants of anticipated conditions ...