While conducting trials, clinical research sites throughout the United States (and sometimes the world) collect necessary data from the trial participants. The Food and Drug Administration (FDA) requires this information from the pharmaceutical companies before the new drug is approved for widespread use by the general public.
Participants in clinical trials are closely observed by a qualified professional research team in order to evaluate the usefulness of the study medication.
Anderson Clinical Research is committed to:
Serving the research interests of our sponsors with integrity
Delivering ethical patient care of the highest quality
Furthering scientific knowledge through excellent clinical trials