The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) announced that it will allow clinical trials of investigational medical products to use electronic signatures when obtaining consent ...

On August 15, 2023, the US Food and Drug Administration (FDA) finalized Informed Consent: Guidance for IRBs, Clinical Investigators, and Sponsors (final guidance). This document finalizes, with new ...

Protecting High-Risk Oncology Patients During the COVID-19 Pandemic by Creating an Isolated Outpatient Clinic Our institution participated in the Oncology Care Model, which required us to include many ...

In today’s digital world, we often desire to have people consent to documents by merely pasting an image of a signature into a document, clicking a virtual button on a web site or mobile phone, or ...