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Hands on – benefit from decades of experience as a Notified Body in our public seminars. In the field of quality management and regulatory issues, we convey the current requirements of EU regulations, EC directives, national laws and standards.

Our experienced and professionally qualified speakers, many of whom are auditors and technical experts with many years of experience, will familiarise you with the content.

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Information event IVDR | Online | Language English

03-26-2025 | 14:00 – 17:00 | Online-Seminar

The long road from IVDD to IVDR – What manufacturers need to consider now

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Being responsible for the seminar area at mdc is a fulfilling task for me, as the medical technology sector is one of the most dynamically growing industries in the world. Innovations, short product life cycles, strict regulations and requirements and new laws make it essential to constantly refresh specialist knowledge. Further training is essential in this sensitive environment in order to keep pace with the constant changes in the industry. Seminars, further education or training courses are a suitable format for passing on knowledge in a practical and focussed manner. Our seminars provide important impulses and up-to-date knowledge about quality management, medical device law or changes due to the Medical Device Regulation. The seminar programme is constantly updated and covers a wide range of further training courses. With up-to-date and well-founded expertise in the field of medical technology, we support specialists in their specific area of interest and provide a practical basis for further developing their own skills.

Our seminars help you to meet the constantly growing challenges and changes in medical technology.
Refresh your knowledge and attend our seminars! I look forward to your participation, and if you have any questions, suggestions or criticism, please contact me personally.

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seminar@mdc-ce.de

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Information event IVDR | Online | Language English

The transition from the IVDD to the IVDR is a complex process for manufacturers of in-vitro diagnostics that brings with it numerous challenges and requirements. Answers to questions and many valuable insights await you at our online info event on 26 March 2025.

Further information