Upcoming Webinar on EU MDR and IVDR Implementation

Save the date for Friday 18 November from 15:30 to 17:00 CET for a unique webinar about implementation of the EU MDR and IVDR in various European member states and recognition of CE marked devices on the UK market, hosted by the Alliance of European Law Firms in which medical devices legal specialists from Spain, Italy, the UK, Germany, Greece, Belgium and the Netherlands will address:

  • A compare and contrast of how competent authorities in the respective countries deal with the concepts of placing on the market and making available under the MDR and IVDR, both crucial concepts for upcoming regulatory deadlines (and maybe some news on where we expect things to go with the MDR and IVDR);
  • A compare and contrast of national implementing measures for the MDR and IVDR, such as regarding sanctions for non-compliance, enforcement policy and specific subjects where the MDR and IVDR allow significant local discretion (e.g. reprocessing of single use devices and as regards in-house produced devices);
  • A compare and contrast of national exemption possibilities under articles 59 and 97 in view of expiring MDD/AIMDD/IVDD certificates and not timely obtain an MDR / IVDR certificate. 

Do not miss out on this unique opportunity to have all your questions about medical devices and IVD regulation implementation in the UK and important EU member states addressed by our expert panel:

  • Francisco Aranega from AMyS Law (Barcelona, Spain)
  • Laure le Calve from LCH Avocats (Paris, France)
  • An Vijverman from Dewallens & Partners (Leuven/Brussels, Belgium)
  • Ioanna Michalopoulou from Michalopoulou & Associates (Athens, Greece)
  • Mathias Klümper and Claudia Lützeler from Lützeler Klümper (Hamburg/Düsseldorf, Germany)
  • Paola Sangiovanni and Flavio Monfrini from Gitti and Partners (Milan, Italy)
  • Alex Denoon and Xisca Borras from Bristows (London, UK)
  • Erik Vollebregt from Axon Lawyers (Amsterdam, The Netherlands)

If you would like to attend, please send us an email to elisabetta.trecani@grplex.com and we will provide you with a link and technical information on joining the seminar well in advance.

Please feel free to share this save the date with colleagues or other people that may find the seminar interesting. If they send us an email, we can send them their own link and information for joining the webinar.

About Paola Sangiovanni

Partner of GITTI and Partners. Seasoned transactional and regulatory legal counsel with a thorough understanding of the life sciences industry.

Leave a Reply

Please log in using one of these methods to post your comment:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out /  Change )

Twitter picture

You are commenting using your Twitter account. Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. Log Out /  Change )

Connecting to %s