For multi-site research, generally the prime awardee is considered the responsible party and must ensure compliance with the posting requirement. The informed consent form must be posted on the ...

Informed consent is one of the primary requirements of research involving human participants. It is important to remember that informed consent is an ongoing process, not a document or single event.

Clinical trials can assist you in getting the right treatment for your condition. Before you consider it, here's what you ...

You're thinking of participating in a clinical trial – what now? Ask questions and weigh the risks before deciding if a clinical trial is right for you.

In addition to understanding informed consent, it is important for researchers to know when to use a waiver and when to use alterations of consent. This UB CTSI Educational Modules video will outline: ...

Obtaining informed consent for trials is not always easy ... Fortunately, the bias of clinical testing may be changing. Almost half of trial participants in America are now women (in the rest ...

Abortion providers had sued the state last year, arguing a ballot proposal passed in 2022 makes certain abortion restrictions ...

Finding a clinical trial that is a good fit can be challenging. Here's how to get the most out of your clinical trial search.

The FDA has approved the first-ever clinical trials for pig kidney transplants in humans marking a breakthrough in tackling ...

Clinical trial complexity, logistical challenges associated with treatments, and resource constraints at trial sites cited as top factors that ...