From 1998 to 2009 I worked as an Engineer and Project Manager for various companies in the medical technology industry. Since 2009 I have attended customers on questions about quality and risk management, biocompatibility and product approvals as a Partner of inmedis, for example:
- Implementation and support of an ISO 13485 quality management system on SharePoint for a
- Supervision of a product development project of a class IIb device from the first idea up to the
creation of the technical documentation and the successful CE registration.
- Analysis and completion of the biocompatibility evidence for the entire product portfolios of international companies in the field of implants, wound treatment and medical equipment
- Upgrade of the quality management system of a medium-sized subcontractor company to MDR-and legal manufacturer level.
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