Why Choose Us
WHY CHOOSE US
​
-
Standard Operating Procedures for clinical trials management
-
QA audit tools and procedures for FDA compliance
-
Competency documentation tools for clinical trials staff
-
Training in the clinical trials industry (GCP & ICH) and FDA regulations for clinical trials staff
-
IATA Certified staff
-
Human Participant Protections Education for all Staff
-
Human Subject Assurance Training for all staff
-
Ongoing review of clinical trials regulations and system adaptation
-
Prompt turn-around of regulatory documents, contracts, and budgets
-
One person contact for all study-related issues
-
Subject recruitment plan and execution
-
Clinical Trial Management System for daily tracking of patient activity
-
Accurate results in a timely manner with data integrity
-
Well trained coordinator staff currently 2 Certified Coordinators and one Certified PI
-
Large database to recruit subjects and patients
-
Use of a central IRB which facilitates timely approval of amendments
-
Great clinic locations (easy access to Highways, Turnpike, Train, & Airports)
-
Demographically, ethnically diverse patient population
-
High enrollment of past studies
-
Extended hours 6 AM - 7 PM, Monday to Friday
-
Open Saturday as needed
-
Adult pharmacokinetics capability (-70� freezer)