We are a multi-specialty clinical research center conducting Phase II, III and IV clinical trials. We help sponsors and pharmaceutical companies develop new and innovative therapies by providing efficient and quality care. We are committed to improving our patients' health and quality of life
We are a research site with 12 full-time research staff members who are completely dedicated and trained to conduct clinical trials. Our study coordinators are Certified Clinical Research Coordinators, GCP trained and IATA certified. We also have a dedicated regulatory specialist to oversee all regulatory documentation requirements and submissions as well as contract and budget staff. Our QA teams closely monitor all activity to ensure that our sites are in compliance with internal and protocol SOPs and regulations. Our qualified staff provides the ability to rapidly contract, obtain IRB approvals, and launch new trials, typically within a matter of days. .
our site
OUR SPACIOUS FACILITY CURRENTLY HAS 3,250 SQ FT OF WORKING AREA AND INCLUDES:
- Four patient exam rooms
- Conference room
- Dedicated coordinator room
- CLIA Certified Clinical Laboratory
- Private office with
workstation specifically designated and equipped for pharmaceutical
company sponsor & monitor use.
- Spacious waiting room with TV
lounge for subjects with comfortable seating.
- Storage space for confidential
patient records and sensitive clinical trial information
- Restrooms
We conduct Clinical Research studies with the help of volunteers like you. By registering with us, we hope that we can find a suitable study for you now, or in the future.