We offer you a wide range of training possibilities. They cover almost all areas of the medical device registration and certification topics. These are for instance the legal and regulatory requirements of the particular target markets (e.g. EU, Canada, USA, Asia, and South America) but also the implementation of normative requirements.

Our medical devices training topics

  • European (EU commission), Canadian (Health Canada) and american (FDA) medical device regulations
  • ISO 13485, ISO 9001 and GMP requirements
  • Country specific requirements

For our current training offerings please check the knoell academy website.

Dr. Albrecht Poth Business Development Medical Devices
+49 621 718858-0 send mail

A global network for medical devices

Our experts and specialists worldwide can help with your individual queries related to medical devices. Get in touch!