answersLogoWhite

0

It is necessary to be able to legally establish that clinical trials are performed with the informed consent of the volunteers, otherwise the company performing the trials could be accused of a very serious crime which violates the Geneva Convention.

User Avatar

Wiki User

12y ago

What else can I help you with?

Related Questions

What has the author T M Grundner written?

T. M. Grundner has written: 'Informed consent' -- subject(s): Forms, Informed consent (Medical law), Medical ethics


Why is there a space for indicating the clinical diagnosis on the laboratory request forms?

A space is provided to specify the clinical diagnosis on their request forms.


When standardized or generic informed consent forms are used they must be used in conjunction with?

a detailed explanation of the study procedures, risks, benefits, and participant rights to ensure that participants fully understand what they are agreeing to. It is important to provide opportunities for participants to ask questions and seek clarification before signing the consent form to ensure they can make an informed decision about participating in the study.


What has the author Jane Dacre written?

Jane Dacre has written: 'The clinical skills matrix' -- subject(s): Ability testing, Clinical competence, Clinical medicine, Evaluation, Forms, Standards 'Clinical skills' -- subject(s): Ability testing, Clinical competence, Clinical medicine, Evaluation, Forms, Standards


Difference between trial master file and site master file of clinial trial?

The trial master file describes the overall conduct of a clinical study and resides at the originating clinical trial coordinating site. In contrast, an individual site file holds site-specific documents describing the conduct of the trial at a specific site including local versions of informed consent forms, patient information leaflets and site-specific submissions and approvals. Versions of the site file will be held at each of the sites participating in a study.


Why is there a space for indicating the clinical diagnosis on the laboratory request form?

A space is provided to specify the clinical diagnosis on their request forms.


Do research participants have to sign consent forms?

Yes.


What are the physicians' requirements for written consent?

By law, the physician who will perform the procedure must explain the risks and benefits of the surgery, along with other treatment options. However, the nurse is often the person who actually witnesses the patient's signature on the consent form.


In terms of explaining the probability of assessment to trial arms in consent forms which is true?

In consent forms, the probability of assessment to trial arms should be clearly explained to ensure participants understand their likelihood of being assigned to each treatment group. This includes detailing the randomization process and how it may affect their treatment options. Clarity in this explanation is essential for informed consent, allowing participants to make knowledgeable decisions about their involvement in the trial. Additionally, it should convey that participation does not guarantee receipt of a specific treatment.


What are the two forms of post-surgical pain?

Pain is recognized in two different forms: physiologic pain and clinical pain


In a veterinary practice blank consent forms are considered to be what?

administrative supplies


Do Jews have consent forms?

Jews first and foremost follow the laws of the land.