Updated 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
Similar opportunities
Service
Legal and Authorized Representation
- MEDICINE
- Consulting
- LIFE SCIENCE
- Certification
Lars Bak-Christensen
Business Development Manager at Lumis International
Berlin, Germany
Service
ISO 13485 Certification Support • 12 Expert Days
- MEDICINE
- LIFE SCIENCE
- Certification
Mhoma NADJIM
Fondateur et PDG at Bio15Pharma
Rouen, France
Partnership
Looking for OR equipment manufacturers seeking a distributor for Italy
- Business
Aldo Truglia
Founder at VEYRA Medical Systems
Rome, Italy