• SKIP TO CONTENT
  • SKIP NAVIGATION
  • Patient Resources
    • Clinical Trial Listings
    • What are Clinical Trials?
    • Become a Clinical Trial Volunteer
    • Useful Resources
    • FDA Approved Drugs
  • Professional Resources
    • Research Center Profiles
    • Market Research
    • Benchmark Reports
    • FDA Approved Drugs
    • Training Guides
    • Books
    • eLearning
    • Events
    • Newsletters
    • White Papers
    • SOPs
  • White Papers
  • Clinical Trial Listings
  • Advertise
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » High Point Clinical Trials Center, Verified Clinical Trials partner

High Point Clinical Trials Center, Verified Clinical Trials partner

February 14, 2017
CenterWatch Staff

High Point Clinical Trials Center has partnered with Verified Clinical Trials (VCT), a global clinical trials database registry, to insure the appropriate selection and qualification of subjects participating in their clinical trials at their North Carolina research facility.

“We are extremely pleased to partner with Verified’s Global Clinical Trials Database Registry to ensure the safety of study participants and continue to provide the highest quality data for our clients,” said Dr. Lorraine M. Rusch, president of High Point Clinical Trials. “It is our medical and quality mandate to use innovative technology such as VCT’s database to prevent the duplicate enrollment of clinical trial participants across multiple trials in different clinical research facilities across the country.”

Duplicate enrollment of subjects (simultaneous enrollment in multiple clinical trials) has become a challenge for the biopharmaceutical sector, impacting clinical research programs across the industry. Verified Clinical Trials uses biometric fingerprint technology to register subjects and create a record of the highest clinical confidence. The result is an improvement in data quality and safety for study volunteers as it prevents duplicate enrollment in trials at facilities in the registry.

“We are proud to welcome High Point Clinical Trials to our client base,” said Mitchell D. Efros, M.D., FACS, CEO of Verified Clinical Trials. “This collaboration demonstrates their commitment to the highest possible quality of participant safety. Including their data in our registry will also significantly enhance the value of the registry to all our participants. Now research sponsors can have an even higher level of confidence in the data High Point Clinical Trials Center provides.”

    Upcoming Events

    • 14Apr

      MAGI 2024: The Clinical Research Conference

    Featured Products

    • Surviving an FDA GCP Inspection

      Surviving an FDA GCP Inspection: Resources for Investigators, Sponsors, CROs and IRBs

    • Best Practices for Clinical Trial Site Management

      Best Practices for Clinical Trial Site Management

    Featured Stories

    • Jonathan Seltzer

      Thought Leadership: Remote Patient Monitoring Gives New View of Safety in Cardiac Clinical Trials

    • Quality_Compass-360x240.png

      Ask the Experts: Applying Quality by Design to Protocols

    • Obesity Treatment Patient

      Clinical Trials Need Greater Representation of Obese Patients, Experts Say

    • Modernize-360x240.png

      FDA IT Modernization Plan Prioritizes Data-Sharing, AI, Collaboration and More

    Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials

    The information you need to adapt your monitoring plan to changing times.

    Learn More Here
    • About Us
    • Contact Us
    • Privacy Policy
    • Do Not Sell or Share My Data

    Footer Logo

    300 N. Washington St., Suite 200, Falls Church, VA 22046, USA

    Phone 703.538.7600 – Toll free 888.838.5578

    Copyright © 2023. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing