It is important that information on clinical studies is available and helpful. Please view the following resources.

Pamphlet For Research Participants

A prospective clinical research patient's guide to reviewing the informed consent document

 

Please contact Goodwyn IRB if you have:

1. Questions regarding your rights as a research participant
2. Complaints or concerns you do not feel you can discuss with the
   study investigator
3. Input or suggestions

IRB Phone: (877) 793-8900 (toll-free
IRB Email: message@GoodwynIRB.com

Past or prospective participants or their designated representatives, and others who wish to obtain answers to questions, express concerns, and convey suggestions, or provide input regarding Goodwyn IRB's Human Research Protection Program may contact Goodwyn IRB at the numbers above at any time.