This article was originally on a blog post platform and may be missing photos, graphics or links. See About archive blog posts. Participation in clinical trials is critical to progress in medicine ...

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

All protocols must detail the informed consent process personnel will use if participants will be involved in the research study. Protocols must use the W&M-approved Informed Consent Form (ICF) linked ...

Clinical research consent forms for certain FDA-regulated clinical trials are now required to contain a specific statement advising participants that clinical trial information will be entered ...

Informed consent is one of the most important aspects of conducting ethical research with human participants. Respecting the autonomy of research participants, the investigator must provide complete ...

Informed consent, which is ethically essential in most clinical research, respects persons’ rights to decide whether participation in the research is compatible with their interests, including ...

Department of Health and Human Services (DHHS) regulations for the protection of human participants require that informed consent information be presented in language understandable to the participant ...

There is no need to utilize the UAB IRB’s Sample Consent form for consent processes in exempt research. Your consent process should be clear and contain full sentences that are in no more than 8th ...

Children are persons who have not attained the legal age for consent to treatments or procedures involved in research; in New York state, anyone under the age of 18 is considered a child. There are ...

Starting today, March 7, 2012, clinical research consent forms for certain FDA-regulated clinical trials must contain a specific statement advising participants that New FDA Research Consent Form ...