






About
Participating
People participate in clinical
research trials for a variety of reasons. In various phases of clinical
research trials, volunteers can gain access to promising medication long
before these compounds are on the market. In addition to gaining access to
medication, volunteers also receive treatment from a licensed physician and
maybe eligible for compensation to assist with travel expenses during the
course of the study.
Clinical Research Associates of Tidewater's goal is to provide good quality
research without compromising the safety and rights of their volunteers.
Patient's rights and safety are protected in two important ways:
First - Any physician awarded a research grant by a pharmaceutical company must obtain approval to conduct the study from an Institutional Review Board. The review board is responsible for examining the study to ensure that the
volunteers rights are
protected, and the study does not present any undue or unnecessary risk
to the patient.
Second - Anyone volunteering to participate in a clinical
trial in the United States is required to sign an "informed consent"
form. The purpose of this form is to provide details about the study,
the risks associated with the study medication, and what procedures the
volunteer will undergo during the course of the study.
Volunteers considering participating in clinical research should discuss it with their primary care physicians or medical caregivers. Also, volunteers should not hesitate to ask the following questions when participating in a clinical research trial:
To express your interest to volunteer, feel free to contact us at any of the following:
24-hour Volunteer Hotline 757-627-6798
402 Medical Tower - 400 Gresham Drive
Norfolk, Virginia 23507
Revised: 06/28/10. Copyright © 2006 Clinical Research Associates of Tidewater. All rights reserved.
Also see...
Volunteer Hotline
757-627-6798
