• SKIP TO CONTENT
  • SKIP NAVIGATION
  • Patient Resources
    • COVID-19 Patient Resource Center
    • Clinical Trials
    • Search Clinical Trials
    • Patient Notification System
    • What is Clinical Research?
    • Volunteering for a Clinical Trial
    • Understanding Informed Consent
    • Useful Resources
    • FDA Approved Drugs
  • Professional Resources
    • Research Center Profiles
    • Clinical Trial Listings
    • Market Research
    • FDA Approved Drugs
    • Training Guides
    • Books
    • eLearning
    • Events
    • Newsletters
    • White Papers
    • SOPs
    • eCFR and Guidances
  • White Papers
  • Trial Listings
  • Advertise
  • COVID-19
  • iConnect
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » Quintiles establishes bioanalytical laboratory in Europe

Quintiles establishes bioanalytical laboratory in Europe

May 7, 2015
CenterWatch Staff

Global CRO Quintiles has expanded its bioanalytical laboratory services with the establishment of a GLP-compliant bioanalytical liquid chromatography-mass spectrometry (LC-MS) lab. The lab, located in the Netherlands, will have extensive bioanalytical testing capabilities and will provide a European facility for Quintiles customers to conduct pharmacokinetics studies. 

The Oss lab facility combines a cohort of employees with extensive industry experience, automated processes and a state-of-the-art facility equipped to increase high-quality throughput. In addition, the lab will bolster and enhance Quintiles' end-to-end clinical trial laboratory services.

"Adding this capability in Europe is a key step for our bioanalytical business and supports the strategy to increase our participation in the substantial European bioanalytical market," said Costa Panagos, senior vice president and global head of global central laboratories at Quintiles.

Currently, Quintiles' bioanalytical and ADME capabilities and work are managed out of three lab sites in the U.S. The new lab will be fully integrated with Quintiles' existing lab in Ithaca, N.Y., enabling the transfer of assays back and forth to accommodate global studies.

As part of Quintiles' bioanalytical and ADME lab services group, the new lab would become part of the recently announced clinical trials lab services joint venture with Quest Diagnostics. That transaction, which remains subject to regulatory approval and customary closing conditions, is anticipated to close in the third quarter. Until that transaction is completed, the new lab will continue to operate as part of Quintiles' bioanalytical and ADME lab network.

"The Oss laboratory will further enhance the scale, clinical trial expertise and diverse therapeutic experience that will be a cornerstone of the proposed joint venture with Quest Diagnostics," said Panagos, who will work as the new joint venture's CEO upon completion of the transaction.  "The addition of the Oss laboratory is integral to the continued evolution of our laboratory business and we're excited about the benefits it can provide as part of a globally scaled and agile business for our customers today as well as in the future."

Upcoming Events

  • 16Feb

    Fundamentals of FDA Inspection Management: Reduce Anxiety, Increase Inspection Success

  • 21May

    WCG MAGI Clinical Research Conference – 2023 East

Featured Products

  • Spreadsheet Validation: Tools and Techniques to Make Data in Excel Compliant

    Spreadsheet Validation: Tools and Techniques to Make Data in Excel Compliant

  • Surviving an FDA GCP Inspection

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

Featured Stories

  • SurveywBlueBackground-360x240.png

    Sites Name Tech Acceptance as Essential Factor in Selection of Sponsors, Survey Finds

  • TrendsInsights2023-360x240.png

    WCG Clinical Research Trends and Insights for 2023, Part Two

  • TimeMoneyEffort-360x240.png

    Time is Money and So Is Effort, Budgeting Experts Say

  • TrendsInsights2023A-360x240.png

    WCG Clinical Research Trends and Insights for 2023, Part Three

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 617.948.5100 – Toll free 866.219.3440

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