ServiceUpdated on 5 February 2025
Certification MDR, IVDR, ISO 13485, MDSAP
Regional Business Unit Development Manager CEE at TUV SUD Polska Sp. z o.o.
Warszawa, Poland
About
For over 30 years, TÜV SÜD has provided certification and testing services for manufacturers and suppliers of medical devices and in vitro diagnostics. We have in-depth knowledge of the medical devices and IVD market and our dedicated team of experts, engineers, and medical doctors provide assessments that cover the full life cycle of your products. We are global, multilingual and have experts in all major markets who provide tailored services based on the industry regulations and requirements.
Type
- Others
Applies to
- Medtech
Organisation
Similar opportunities
Service
International market access (from EU to US and China)
- Medtech
- Consulting
- Development
- Manufacturing
- Biotech and Lifescience
Liang (Antonio) Dr. Li
Founder at Medkaizhen
Ulm, Germany
Service
Notified Body (EU) 2017/745 MDR
- Others
- Medtech
Vasily Kalakutskiy
Medical Product Certification Business Development Manager at SGS Germany GmbH
Puchheim, Germany
Service
Product Classification and Categorization
- Consulting
Tabatha Bourgois
Director, Regulatory and Clinical Development at Alira Health
Barcelona, Spain