Effects of the coronavirus disease 2019 pandemic on anxiety and spirituality in patients with cancer undergoing chemotherapy: A cross-sectional study. This is an ASCO Meeting Abstract from the 2023 ...

Obtaining valid consent is a fundamental part of providing quality care and a key ethical and legal requirement in medicine. Issues around consent can, however, trip up even the most experienced ...

Canadian researchers have published new guidelines intended to make consent forms used in clinical research easier for patients to understand. The guidelines describe 75 core elements for consent ...

New patient consent forms in Germany cover the use of patient care data and clinical and biomedical research. German Data Protection Commission DSK has approved a revised version of forms that the ...

Expedited studies are research projects that meet one of the categories under 46.110 and involve minimal risk. Full board studies are those the IRB determines does not fall under exempt or expedited ...

Informed consent is a process that’s required for most medical procedures. However, there’s often confusion about what informed consent is, what it means, and when it’s needed. In a healthcare setting ...