Crash Course Medical Devices – How to Avoid Typical Pitfalls
New product ideas and technologies in the healthcare sector are more in demand than ever – technological change is enabling rapid progress in a growing industry. For many founders and scientists, startups and young companies, interesting market niches are forming here. The field is wide: from medical instruments to novel dressings, laboratory diagnostics and products for injection or transfusion and dialysis to implants, 3D printed tissues, drug components or new software solutions.
Prepare for the market launch as early as possible
In order to prepare the market launch of new services and products as well as possible, relevant criteria must be considered from the outset with regard to the requirements of approval and regulatory hurdles.
Peter Diesing, Head of Certification Medical Device at Eurofins Product Service GmbH, explains typical pitfalls and answers important questions – from approval and technical documentation to the testing of medical devices – as part of a three-part, free seminar series.
Participants will have the opportunity to clarify individual questions and exchange ideas with like-minded people.
The crash course dates
21. April 2021, 10.00 bis 11.30, online
Approval of Medical Devices – Crash Course: How to Avoid Typical Pitfalls
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28. April 2021, 10.00 bis 11.30, online
Technical Documentation of Medical Devices – Crash Course: How to Avoid Typical Pitfalls
Crash course: How to avoid typical pitfalls
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5. Mai 2021, 10.00 bis 11.30, online
Medical Device Testing – Crash Course: How to Avoid Typical Pitfalls
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