A clinical trial is a research study to answer specific questions about investigational treatments or new ways of using known treatments. It is a test to see if the investigational treatment is safe and effective.
All aspects of the treatment and the clinical trial process is governed and overseen by the Food and Drug Administration (FDA).
Doctors and research facilities run the tests according to strict guidelines and rules. The FDA monitors clinical trials very closely to maintain that all safety guidelines are followed.
South Florida Medical Research has two full time Certified Data Coordinators who are experienced in handling all aspects of clinical trial regulatory documents and procedures.
We pride ourselves in being thorough, efficient, and accurate in our reporting and documentation efforts.
We strive to meet all FDA IRB, and sponsor requirements in a timely manner. Patient safety and care are our priority.
For information on regulatory procedures or documentaion you may call 305-931-8080 or email the office at Info@southfloridamedicalresearch.com