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The Future of Swedish & Danish Life Science and Med-Di-Dia

29/8/2023

The Future of Swedish & Danish Life Science features a highly topical seminar programme, pre-bookable one-on-one partnering meetings, excellent facilities for informal networking, as well as a lively exhibition. These four core elements run in parallel in order to guarantee our visitors an energetic full-day experience, designed to inspire, spread knowledge and promote new and important collaborations.

 

The event attracts between 400 and 500 leading decision-makers from all over the world, annually. The participants come from the pharma, biotech and medtech sectors; the academic research and the healtchcare sectors, as well as policy makers, regulatory authorities and the financial services sector.

 

Our Regulatory and Quality Compliance Expert – Dr Shahram Ahmadi, will be attending this event and you will have an opportunity to get answers regarding:

  • EU MDR / IVDR Timeline and Transition
  • Launching your Medical Innovation in the EU, UK, USA and ROW
  • Appointing an EU Authorised Representative [EUAR]
  • Appointing a Person Responsible for Regulatory Compliance [PRRC]
  • Post Market Surveillance requirements for Medical Companies
  • Quality Management Systems
  • Risk management Plans

Any and everything related to Regulatory and Quality Compliance requirements for Medical Devices, Diagnostics and Digital Health!

 

Register for the Event – by clicking on this Registration Link

Do you have any questions for our expert? Ask them by sending an email to mdd@mddltd.com or by visiting this link.

 

 

Regulatory Support at The Future of Swedish & Danish Life Science and Med-Di-Dia

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