North America Research Institute

08/16/2022

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02/23/2021

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Connect with top nephrologists and the latest in research opportunities near you.

12/02/2020

Here is some great information from one of our Sponsors on COVID-19 and Clinical Trials

12/01/2020

Give us a call today! :)

11/23/2020

09/30/2020

For more information, please give us a call at 1-800-797-1695 x 118 or visit Brightnstudy.com

09/29/2020

What is Informed Consent in Research?
Informed consent is the process of learning the key facts about a clinical trial before deciding whether or not to participate. It is also a continuing process throughout the study to provide information for participants. To help someone decide whether or not to participate, the doctors and nurses involved in the trial explain the details of the study. If the participant’s native language is not English, translation assistance can be provided. Then the research team provides an informed consent document that includes details about the study, such as its purpose, duration, required procedures, and key contacts. Risks and potential benefits are explained in the informed consent document. The participant then decides whether or not to sign the document. Informed consent is not a contract, and the participant may withdraw from the trial at any time.

09/25/2020

Patients are waiting. That is what motivates Mayo Clinic’s researchers in their quest for better treatments and cures. Clinical trials bridge the gap between...

09/21/2020

to learn more, give us a call! 1-800-797-1695 ext 118 or visit https://brightnstudy.com/

12/06/2017