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)

RAPID STARTUP

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EXPERIENCE

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QUALITY ASSURANCE

FACILITY

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Ph: (803) 531-2220

Fax: (803) 531-2270

3709 Magnolia St
Orangeburg, Orangeburg County 29118
USA

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