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16 – 29 Nov 2026 | Düsseldorf, Germany

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ServiceUpdated on 12 October 2026

CE Certification and Regulatory Services

Business Development Manager at Lumis International

Berlin, Germany

About

Lumis International (Germany) helps medical device manufacturers achieve EU market entry — CE marking under MDR/IVDR, technical documentation, clinical evaluation support, and Authorized Representative (EC-REP) services. We guide you through the full regulatory pathway to market access, helping you avoid the delays common under the current MDR framework. If you're planning or expanding your EU presence, let's connect at BIOSPAIN to discuss your device's regulatory strategy and timeline.

Type

  • Certification
  • Consulting
  • Other

Applies to

  • LIFE SCIENCE
  • MEDICINE

Organisation

Lumis International

Consulting (business, tax, legal)

Berlin, Germany

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