Our Center:
We are a dedicated research site that are able to conduct clinical trials Phase I-IV with over 15 full-time research staff members who are completely dedicated and trained to conduct clinical trials. Our study coordinators are GCP trained and IATA certified.
Our physicians are Board Certified including Pulmonologist, Internists, Hospitalists, General Doctors, Family Doctor, Surgeons, Gynecologists, Psychiatrist, Psychologists, and Neuro-Psychologists, GCP Certified and are Certified in Human Subject Protection Regulations.
In addition, 3 Nurse Practitioner and 2 Registered Nurses. We also have dedicated regulatory specialists to oversee all regulatory
documentation requirements and submissions as well as contract and budget staff.
Our Quality Control team 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.
We count on four patient exam rooms CLIA Certified Clinical Laboratory Large conference room Dedicated coordinator room
Private office with two workstations specifically designated and equipped for pharmaceutical company sponsor and monitor use
Two waiting rooms with TV lounge for subjects with comfortable seating and personal computer with high-speed internet access.
Ample storage space for confidential patient records and sensitive clinical trial information.
All study drug is kept in a secure medication room Storage is kept locked at all times and is only accessible to assigned clinical personnel by individual key card access. Limited access is strictly enforced.
Refrigerators, -20 & -80°C Freezers 24/7 Electronic Temperature Monitoring System with Alarm Refrigerated and standard centrifuges
ECG machines Backup generator in case of power failure High-speed wireless internet access throughout Our clinical staff is reliable and highly trained, with over 30 years of experience. We are actively recruiting individuals willing to participate in current and upcoming clinical trials.