A civil trial opened Thursday on a challenge to abortion restrictions that remain on the books in Michigan. We have more from ...

Speakers at MediaNama's event on draft DPDP Rules discussed consent notices, data summaries, and how companies should approach compliance.

These are tools used by the IRB and are not required to be used/submitted by investigators. Research teams may find them helpful when writing protocols to more clearly understand what the IRB must ...

Introduction: Informed consent is a cornerstone of modern clinical ... Eligible studies included surveys, focus groups, or interviews. Based on a review of consent form templates, we identified 18 ...

In the coming months and years, clinicians and policymakers in the US should heed the HHS directive to protect the informed consent rights of their patients with intersex variations. Human Rights ...

But United’s first two games of 2025 have, at the very least, offered a template from which they can build. Two full weeks on the training ground to prepare for those matches clearly helped but ...

We are working with Guy’s and St. Thomas’ NHS Foundation Trust to produce national standardised SACT regimen-specific consent forms. We want to support clinicians in ensuring all patients are fully ...

You're required to have all participants in your study complete an Informed Consent Form. See an example of an Informed Consent Form (pdf). Below are the Bethel University Institutional Review Board’s ...

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