🇨🇿 EUDAMED: Last Call – Requirements to meet by May 28, 2026?

The event is held in Czech language only!

As of May 28, 2026, following numerous delays, the EUDAMED database will become mandatory for all relevant economic operators. Active use and filling of the EUDAMED database is associated with a number of significant benefits for the entire medical device and IVD sector; however, fulfilling registration obligations during the short transition period is also accompanied by a significant administrative burden, particularly for medical device manufacturers. The aim of our webinar will be to present practical and clear guidance on how to ensure compliance with all relevant obligations in the remaining time, given the upcoming deadlines.

The presentation will focus primarily on the practical aspects of fulfilling individual obligations and will demonstrate how to perform specific mandatory activities directly within the database environment. Specifically, we will focus on obligations related to the registration of economic operators; a significant portion will be devoted to the execution of registration for all types of medical devices as well as the specific obligations of importers. Last but not least, we will focus on methods to reduce the administrative burden, such as bulk data uploads to the database or avoiding potential errors during the registration process. 

Who the webinar is for:

• Regulatory specialists at manufacturers and systems and procedure packs producers

• Staff in Quality management and PRRC departments

• Regulatory specialists at importers and distributors

• Healthcare providers and other users who wish to use data from the EUDAMED database for their own work

Lecturers:

• Ing. Jakub Musil

• Ing. Terézia Vedral

Content:

• EUDAMED and its legal basis in the MDR and IVDR

• A practical overview of obligations for all roles of economic operators (Actors)

• An overview of the deadlines by which obligations must be met

• The relationship between the EUDAMED database and national-level databases (ISZP, RZPRO)

• The economic operator registration process (“Actor registration” module)

• The process of linking to non-EU manufacturers for importers

• The medical device registration process (“UDI/Devices registration” module)

• Bulk data upload to the EUDAMED database – practical advice and tips

  
  

Additional information:

• During the webinar, participants will have the opportunity to ask questions

• Each participant will receive a certificate of participation

• A PDF presentation will be sent to all participants

Participation fee:

• 3.900 CZK excluding VAT

• 100% cancellation fee applies after bindingly confirmed registration, but with the possibility of sending a replacement participant

Webinar hosted by:

• Porta Medica s.r.o.

• ID: 03301931, VAT: CZ03301931

• Registered office: Opletalova 1525/39, 110 00, Prague 1 - Nové Město