Medical Device Development

With our multidisciplinary team of highly qualified experts, we offer professional service throughout the development process of medical devices. From project management to the preparation of the complete technical documentation, we ensure that you meet the regulatory requirements and get your medical device worldwide registered in the most shortest time frame.

  • Medical Device & Drug Combination Development

  • CE Mark & FDA registration

  • Project Management

  • Design Verification and Design Validation

  • Preclinical Testing

  • Prototype development

  • Design History File

  • Risk Management 

  • Clinical Evaluation 

  • Biocompatibility 

  • Usability and Human Factor Engineering 

  • Post Market Surveillance 

 

 

 

 

We support companies in the development of medical devices to meet MDR and IVDR  compliance and to shoorten time of CE mark approval.

Contact

Bellingswood Group GmbH

Thurgauerstrasse 117

8152 Glattpark - Zürich

Switzerland

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Tel: +41 79 85 84 825

info@bellingswood.com

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© 2019 by Bellingswood Group GmbH