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