Updated on 12 October 2026
Legal and Authorized Representation
Business Development Manager at Lumis International
Berlin, Germany
About
Lumis International (Germany) helps non-EU MedTech and biopharma manufacturers achieve EU market entry — CE marking, MDR/IVDR compliance, and Authorized Representative (EC-REP) services. We support companies from initial regulatory strategy through to CE certification and post-market compliance, with particular experience guiding non-EU manufacturers into the EU. If you're planning or expanding EU market access, let's connect at MEDICA to discuss your regulatory pathway and timeline.
Type
- Certification
- Consulting
Applies to
- LIFE SCIENCE
- MEDICINE
Organisation
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Service
CE Certification and Regulatory Services
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- MEDICINE
- Consulting
- LIFE SCIENCE
- Certification
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