IRB
Clinical Pharmacology of Miami, Inc has many years of experience with many different IRBs. Our dedication to protect the safety, ethical concerns and rights of our volunteers is sincere. We strive to to be up to date and in compliance with all regulatory agencies, including the US Food and Drug Administration.

We employ the services of several IRBs, including any central IRB that is recommended by the sponsor. Most commonly we utilize either Independent IRB or Integreview. Within our research unit facility, we specifically designed suitable interview rooms to perform the informed consent process in a professional and confidential environment.

For more information regarding our IRBs, please follow the links below:
WWW.IIRB.COM
WWW.INTERGREVIEW.COM