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DRG® USA CORPORATE HEADQUARTERS

DRG® MISSION STATEMENT

DRG International, a global innovator of high-quality medical diagnostics and equipment,  provides the medical and research community with cutting edge, effective tools to build a healthier future.

 

DRG International, Inc., founded in 1970 is a multinational specialty medical equipment and diagnostics manufacturer and distributor with successful representation in over 110 countries through a network of DRG® Subsidiaries and local distributors. The highly skilled DRG® Staff of medical, clinical, marketing and service specialists are experienced in supplying cost effective innovative products and systems to our customers Worldwide.


Located 18 miles West of New York City, DRG® Corporate Headquarters provides logistic and financial management support to DRG® Subsidiaries overseas and coordinates the DRG® distributor network. An experienced, multinational, multilingual staff is ready to serve your medical and diagnostic products needs Worldwide.

For a copy of the DRG® Corporate Profile please click here.

 DRG Instruments GmbH Awarded ISO Certification

DRG International, Inc. is pleased to announce that its German facility, DRG Instruments GmbH holds ISO Certificates by the Certification Body of the TUV Rheinland Product Safety GmbH. The certification established and applies a quality management system for medical devices for the scope of Design and Development, Manufacture and Distribution of in vitro Diagnostics by Enzymeimmunoassays (ELISAS) and Radioimmunoassays (RIAS) Technology.

DRG Instruments GmbH's quality management system is certified according to:

ISO CERTIFICATES ISO CERTIFICATES PRODUCTS COVERED BY ISO
EN ISO 9001-2008 SO 13485 CMDCAS 12-12_CE_DEC_List_B
EN ISO 13485:2003+AC:2007 ISO_9001-2008_EN 2013-04_CE-DEC_Miscelleneous_Products
ISO 13485:2003 under CMDCAS ISO_13485-2012_EN  
ISO 13485:2013 under CMDCAS ISO_List_B_EN  

 

 

(you can review DRG® Certifications by clicking in the links above).

Furthermore, DRG Instruments GmbH  is in full compliance with the current EU guideline for Directive 98/79/EC Annex IV, Article 3 Full Quality Assurange System for in vitro diagnostic medical devices.

 

DRG® is listed in the following directories:


               CLR      

     LMI                         Linscott's                 

  American Society for Clinical Laboratory Science

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