Research Centers of America’s early phase team’s experience lies in special population and complicated healthy volunteer trials.

Our multi-specialty site leads the industry in executing highly-detailed studies with board-certified physicians at the helm.  To ensure subject safety protocol specific trainings and dry runs are conducted prior to study start.  ACLS-certified staff is present and a physician is on call throughout admissions.  Emergency medication and equipment are easily accessible and regular drills are conducted.

Our clinical research experience covers a variety of indications, including Alzheimer’s, Arthritis, Classroom Simulations, Dermatology, Diabetes, Hepatic and Renal Impairment, Hypogonadal, Oral Contraception, Parkinson’s, and Post-Menopausal populations.

Subject retention is of the utmost importance.  Our site develops instruction sheets for subjects with projected visits dates/important notes.  Additionally, reminder calls are made to partcipants throughout the trial.  Establishing a good rapport between subjects and the study team is also key.  This is achieved through early subject education and a unit orientation upon admission.

 

Successful trial execution in the following areas:

  • Bioavailability/Bioequivalence
  • Biologics / Biosmilar
  • Drug-to-Drug Interaction
  • First-In-Man
  • Food Interaction
  • PK/PD
  • QTc/Cardiac Safety
  • SAD/MAD