MedtecLIVE | Services in biomedical engineering
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Services in biomedical engineering

Today, medical device manufacturers are faced with demanding requirements when developing their products.

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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
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Be there as an exhibitor

You can conveniently book your stand at MedtecLIVE via our online stand registration.

Do you have any questions? Please contact us

Jessica Nether und Silke Ludwig

MedtecLIVE Sales-Team

Jessica Nether and Silke Ludwig

We will be glad to advise you.

medteclive@nuernbergmesse.de +49 9 11 86 06-85 44

To all exhibition topics

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All exhibiton topics

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Design, R&D

In medical technology design, it is necessary to find the balance between many requirements and a nevertheless unusual device design.

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IT in medical technology

Digitalisation is becoming ever more important in biomedical engineering, with various laws laying out the legal framework in e-health.

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Materials and Components

Modern biomedical engineering uses a variety of materials that must perfectly meet the needs of the respective application.

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Processes, Mechanical Engineering, Manufacturing & Automation

Speak with our exhibitors and discover how they can help you in the processes involved in medical device production.

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Measurement, Testing, Validation

Testing innovations in medical technology is an essential part of product development and approval.