U.S. markets open in 2 hours 42 minutes
  • S&P Futures

    4,280.50
    -27.25 (-0.63%)
     
  • Dow Futures

    33,965.00
    -153.00 (-0.45%)
     
  • Nasdaq Futures

    13,557.25
    -101.00 (-0.74%)
     
  • Russell 2000 Futures

    2,009.90
    -13.40 (-0.66%)
     
  • Crude Oil

    87.11
    +0.58 (+0.67%)
     
  • Gold

    1,787.40
    -2.30 (-0.13%)
     
  • Silver

    19.88
    -0.21 (-1.05%)
     
  • EUR/USD

    1.0175
    +0.0004 (+0.04%)
     
  • 10-Yr Bond

    2.8240
    0.0000 (0.00%)
     
  • Vix

    20.43
    +0.48 (+2.41%)
     
  • GBP/USD

    1.2098
    +0.0004 (+0.03%)
     
  • USD/JPY

    134.8990
    +0.6840 (+0.51%)
     
  • BTC-USD

    23,774.19
    -275.63 (-1.15%)
     
  • CMC Crypto 200

    566.51
    -5.41 (-0.95%)
     
  • FTSE 100

    7,506.09
    -29.97 (-0.40%)
     
  • Nikkei 225

    29,222.77
    +353.86 (+1.23%)
     

Agilent Releases IVDR-Compliant Instruments, Kits, and Reagents for Use in the European Union

  • Oops!
    Something went wrong.
    Please try again later.
  • Oops!
    Something went wrong.
    Please try again later.
·2 min read
In this article:
  • Oops!
    Something went wrong.
    Please try again later.
  • Oops!
    Something went wrong.
    Please try again later.

SANTA CLARA, Calif., June 01, 2022--(BUSINESS WIRE)--Agilent Technologies Inc. (NYSE: A) today announced that previously CE-IVD marked instruments, kits, and reagents were released as IVDR Class A on May 26, 2022, in compliance with the new EU IVDR regulation.

This launch of IVDR-compliant Class A products ensures that labs in the EU who rely on Agilent IVDR instruments, kits, and reagents in their diagnostic workflows will continue to be able to use these products without disruption.

The In Vitro Diagnostic Regulation (IVDR) (EU) 2017/746 is a new, harmonized regulatory framework established to ensure the present and future safety and performance of in vitro diagnostic (IVD) medical devices in the European Union market. The IVDR regulation replaces the previous IVDD directive, under which many Agilent products have been CE-IVD marked, indicating IVDD compliance. The launch represents a significant milestone for the Agilent organization, which faced substantial hurdles due to the COVID pandemic and related supply-chain challenges.

"Agilent shares the European Commission's vision of enhanced patient safety and transparency," said Jenipher Dalton, senior vice president of Global Quality and Regulatory Affairs at Agilent. "We remain committed to providing high-quality solutions for delivering the testing results that physicians and patients in the EU rely on. Our multi-disciplinary team really came together to make this a seamless transition, and this result is a testament to their dedication and professionalism."

Agilent Class A IVDR-compliant products span the entire Agilent product portfolio, from qPCR and NGS preparation instruments to H&E stains, staining instruments, and conjugated secondary antibody reagents.

About Agilent Technologies

Agilent Technologies Inc. (NYSE: A) is a global leader in the life sciences, diagnostics, and applied chemical markets, delivering insight and innovation that advance the quality of life. Agilent’s full range of solutions includes instruments, software, services, and expertise that provide trusted answers to our customers' most challenging questions. The company generated revenue of $6.32 billion in fiscal 2021 and employs 17,000 people worldwide. Information about Agilent is available at www.agilent.com. To receive the latest Agilent news, please subscribe to the Agilent Newsroom. Follow Agilent on LinkedIn, Twitter, and Facebook.

View source version on businesswire.com: https://www.businesswire.com/news/home/20220601005431/en/

Contacts

Naomi Goumillout
Agilent Technologies
+1.781.266.2819
naomi.goumillout@agilent.com