The Initial Protocol Application, like all of the HRPP webforms, is an interactive form with built-in logic. That means that the answers to some questions will reveal other questions. Only the ...

The Revised Common Rule requires all clinical trials to post an unsigned consent form on a publicly available website. The Revised Common Rule is in effect for studies approved on or after January 21, ...

Ethicists have suggested that written consent forms encourage participants in phase 1 cancer trials to expect benefit from the experimental agent and to overlook serious risks. Of 272 forms, 268 ...

Please provide your email address to receive an email when new articles are posted on . Informed consent forms for interventional oncology clinical trials are often lengthy and written at too high of ...

The three sample GDPR texts will provide a customizable framework for your organization to use and stay compliant. Constantly Updated — The download contains the latest and most accurate details.

In what seems to be an increasing phenomenon, injured plaintiffs/insureds are being asked to sign Consent Forms when they attend a tort defence medical examination or an insurer examination (“IE”) ...