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• News and events
  • 2018
• About LNE/G-MED
  • Brief history
  • Legal status
  • Organization and management
  • Activities
  • G-MED North America
  • Addresses & Contacts
• Services
  • CE marking
  • Certification of Company Management Systems
  • Quality certification of sterilization processes
  • MDSAP certification
  • Access to the American market
  • Access to the Taiwanese market
  • Access to the Australia and New Zealand markets
  • Access to the Japanese market
  • Medical equipment :
    CB Scheme certification
  • Product certification
  • Training
• Applying for certification
  • How to obtain certification
  • Receive a detailed proposal
  • Additional information
• Certified companies or bodies
• Recognition and accreditation
• Guides
  • CE Marking : Dealing with changes in medical devices
  • IEC 60601 3rd edition
  • Electromagnetic Compatibility (EMC)
  • Registration medical device in Brazil
  • Japanese Medical Device Approval Process
  • How to change your Notified or Certification Body
  • Presentation of biological evaluation According to ISO 10993-1
• Links to key sites
• FAQ

Brief history

1979

Medical equipment test laboratory group GLEM is formed.

1994

Medical device assessment body G-MED is set up as an economic interest grouping (GIE). The four G-MED partners are the French Ministries of Health and the French Ministry of Industry, the Laboratoire Central des Industries Electriques (LCIE) and LNE.

1998

G-MED restructures with LCIE and LNE as its two sole partners.

2000

LNE/G-MED opens a regional office in Saint-Etienne.

2004

All G-MED activities performed by LCIE are transferred to LNE.

2005

The economic interest grouping is dissolved and LNE becomes the sole certification body and notified body. The G-MED name and logo are retained.

The G-MED North America subsidiary is set up in Washington DC.