How it work?
Participating in a Clinical Research Study is Easy
Participating is Easy!
Potential Patient Pathway
For those interested, we make it easy to get started and verify eligibility.
Pre-selection
At this stage, we address the specific inclusion/exclusion criteria for the study and other suitability issues. A telephone interview may also be required for qualification.
Selection
At this stage, you will receive a study consent form (ICF). You will meet the physicians and clinical coordinator. A physical evaluation and review of your medical history is often required. A waiting phase may also be required.
Registration/Randomization
Once we qualify you, treatments will begin, and you will also be randomly assigned to receive one of several clinical interventions that could be placebo. You and your doctor may not know what you are getting.
Treatment Period
During the treatment period, we will be monitoring your progress and adverse event assets. Depending on the study, follow-up visits, laboratories and electrocardiograms may be required or needed.
Final Phase / Final Treatment
When your testing is complete, you will have a final required safety visit, plus labs, physical assessments and adverse events attached.
Help us to Discover
The Future Of Medicine!
Explore our available studies and see if there is one that fits your needs.