The purpose of informed consent is to make sure you make an educated choice about your clinical trial participation. There is more to the process than simply asking you if you agree to participate.

Informed consent is vital for any clinical trial. However, the length and complexity of consent information can lead to patients misconstruing key points and failing to understand the implications ...

Once they have completed the evaluation, they can download their course certificate. This means there is an almost 100% return on evaluation as the researchers need to provide evidence – the ...

It is not enough to enhance efficiency or accuracy; we must embed transparency, temporal awareness and systemic oversight ...

Discover what clinical trials are, why they're vital for new treatments, and how you can participate in life-changing medical ...

In a first step toward FDA approval of kidney xenotransplantation, a living human with end-stage kidney disease may receive a ...

Discover how young healthcare innovators from Durban are transforming clinical trials and community health, earning accolades ...

Clinical trials make it possible to apply the latest scientific and technological advances to patient care. ... Informed Consent. Informed consent means that as a patient, ...

Through the inFormed Consent App, patients are able to watch recordings of investigators explaining the clinical trial and ask questions. The app records them as they do so it can capture them ...

With technology/AI taking over administrative and repetitive tasks, human roles will shift towards more strategic, creative, ...

Dynamic consent provides personalised online platforms which enable the attainment and management of informed consent and allow ... It isn’t abnormal for clinical trials to require costly ...

Consent for Clinical Trials. Informed consent is communication between a patient and provider in which the patient is given information about and understands their condition, their treatment options, ...