Managing a
heart or kidney
condition?

Clinical trials are conducted under very careful supervision by the pharmaceutical companies and the FDA during and throughout the studies, and according to strict guidelines outlined prior to starting any study. Volunteer safety and health status information is carefully monitored via physician and research coordinators as well as by pharmaceutical company representatives throughout each study participation and follow-up period.

Approval by an independent Institutional Review Board (IRB) is required prior to and throughout the course of every research study. The IRB is dedicated to the protection of study volunteers and includes members of the medical and legal professions as well as the general public (such as religious leaders, social workers, and well informed citizens).

Study volunteers are at the heart of our business at Injury Care Research and Family Care Research. Benefits to volunteering include careful evaluation of your personal health by a team headed by physicians renowned in their field of expertise. Participating in a clinical trial gives you the opportunity to receive new therapies before they are made available to the general public, as well as the knowledge that you are making a personal contribution to the advancement of global health care.

No. Not only will your care and related medications be provided at not cost to you, you will be compensated for your time and travel associated with your participation.

Yes, you can still participate. Insurance is not needed.