Coastal Carolina Research Center is constantly revisiting and perfecting our Standard Operating Procedures (SOPs). Currently our SOPs include the following:

Informed Consent (includes process for vulnerable populations, other special populations and the assent process) Serious Adverse Events Non-Serious Adverse Events Investigational Product Control & Accountability Investigational Product Transfer Control & Accountability of an investigational product that is a Controlled Substance Drug Destruction Laboratory Procedures Transport of Laboratory Specimens from offsite location Use of Health Information of Actual or Potential Study Patients Lost to Follow-Up Patients Time-Sensitive Trials Safeguarding Personal Health Information Using “Previously Signed by Investigator” Stamp Pre-study Evaluation Instructions for all Potential Study Volunteers and/or Health Screening Participants Obtaining Height and Weight Health Screenings Equipment Calibration

If you would like more details about a potential clinical study opportunity with Coastal Carolina Research Center please contact:

Nathan Morton
Director of Business Development
Phone #: 843-856-3784
Fax #: 843-856-3788
Email: nmorton@coastalcarolinaresearch.com

Study Experience
PI Experience
Sponsors Experience
CRO Experience