Ing. Alexander Maier

Key responsibilities: MDD, MDR, Product authorisation, ISO 13485:2016, 21 CFR 820, MDSAP, CE marking • Preparation of relevant documents for national and international registration and check for conformity • Monitoring of relevant standards and adaptation of technical documentation • Support the product development in all aspects of documentation in accordance with applicable standards and guidelines • Evaluating current and new products for compliance with applicable regulations

Development of a multichannel and electromechanical connector for in vivo applications (1.3)

Development and characterization of solder connections for module interconnection of galvanically metallized silicon solar cells (1.0)

Biomedical Engineering