• Clinical Trial Organization
    • Study device logistics
    • On-site clinical support
    • Monitoring
    • Support for all legal notifications
  • CE- Certification Support
    • Compile a medical device CE Marking
    • Technical File Register medical devices with the EU Competent Authority
  • EU Authorized Representative Services
    • Gives you authorization to place our name and address on your device labels, packaging and
    • Instructions for Use. Protects the confidentiality of your documentation. The European Authorized
    • Representative can only show technical documentation to Competent Authorities as required by law.

Are you looking for a partner, who represents your company and products on the German-speaking market for medicine technologies successful and competent?

As distributor we can present our clients the whole range of performances of an efficient marketing organization. We have many years of experience particular in cardio surgery and all spheres of activity adjacently, as well as an excellent knowledge of the markets and that we are more closely to your customers, amount to considering us as a powerful partner to your company.

If start-up or already established, we care for your market penetration in the German-speaking area.



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