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Services in biomedical engineering
Today, medical device manufacturers are faced with demanding requirements when developing their products.
Services in biomedical engineering
They must comply with all medical regulations in full before the product can even go to market. These are accompanied by several norms, standards and processes like the European Medical Devices Regulation (MDR) and the In-Vitro Diagnostic Devices Regulation (IVDR). In order to succeed, medical technology manufacturers rely heavily on the training and expertise of their staff.
- Regulatory Affairs
- Documentation
- Consulting
- Marketing / sales
- Patents & IP
- Approval
- Certification
- Financing / sponsorship
- Translation
- Recruitment agency
- Cluster / associations / lobby groups
- Publications
- Continuous education / training
- Quality assurance and control
- Other
Do you have any questions? Please contact us
MedtecLIVE Sales-Team
Jessica Nether and Silke Ludwig
We will be glad to advise you.
medteclive@