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Events

Stay up-to-date with the latest events in regulatory compliance and our agency offerings by checking out our event calendar. We offer a variety of events, including webinars, conferences, and more, to help you stay informed and improve your skills and knowledge in all medical device regulatory matters.

Upcoming Educational Events

Calendar

June 2025
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Tue
Wed
Thu
Fri
Sat
Sun
26
0:00
Deadline Lodge an Application for IVDR Conformity Assessment for IVDs Class D
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27
28
29
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31
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16
9:30
🇨🇿 Practical guide to the EUDAMED database: obligations, deadlines, registration
+1 more
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30
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Past Events

  • 16 Jun 2025, 09:30 – 12:00
    Online: Cisco Webex
    The online seminar is intended for manufacturers, kit assemblers, importers or distributors of medical devices, but also for other entities that are actively addressing the issue of compliance with EU legislative requirements in connection with the launch of the EUDAMED database.
  • 26 May 2025, 00:00
    Europe
    Deadline to lodge an application for IVDR conformity assessment for IVDs that would become Class D under IVDR in order to benefit from extended transition period.
  • 26 May 2025, 00:00
    Europe
    Deadline to have IVDR QMS in place (in accordance with Article 10/8 IVDR) for IVDs (all classes) that want to benefit from extended transition period.
  • 13 May 2025, 09:30 – 12:00
    Online: Cisco Webex
    The webinar focuses on the rules of advertising of medical devices and IVDs from the perspective of Czech and EU law. You will learn how advertising addressed to professionals differs from advertising aimed at the general public and we will introduce you to the changes that are planned in this area.
  • 06 May 2025, 09:30 – 12:00
    Online: Cisco Webex
    An online seminar for all medical device suppliers participating or considering participating in a medical device procurement. You will learn how to submit a stress-free, error-free bid from a medical device regulatory perspective and increase your chances of success in the procurement process.
  • Tue 15 Apr
    15 Apr 2025, 09:30 – 12:00
    Kancelář Porta Medica, Opletalova 1525/39, Nové Město, 110 00 Praha-Praha 1, Czechia
    A face-to-face seminar designed for all medical device suppliers considering inclusion of their ZUM products in the VZP-ZP Reimbursement Catalogue. Participants will gain an overview of the procedure, key documentation requirements and practical steps for successful submission of a proposal.
  • 09 Apr 2025, 09:30 – 12:00
    Online: Cisco Webex
    This webinar is prepared at the request of participants of our educational events, who approached us with a request to hold an event at least once every six months, focused on a executive summary of the important changes that have taken place in the regulation of medical devices.
  • 01 Apr 2025, 09:30 – 12:00
    Online: Cisco Webex
    A webinar for importers and distributors who want to clarify what obligations currently apply to them. It will focus on duties under the EU MDR and IVDR regulations and good storage practices. Issues will be illustrated with examples from practice and part of the webinar will be dedicated to news.
  • 19 Mar 2025, 08:30 – 11:30
    Online: Cisco Webex
    An online seminar that will focus on good practice in the management of medical devices in the hospital environment. The seminar will provide an overview of current legislative requirements, highlight the most common problem areas and offer practical solutions for day-to-day operations.
  • 11 Mar 2025, 09:30 – 12:00
    Online: Cisco Webex
    The webinar is intended primarily for sales staff of medical device suppliers, hospital purchasers, representatives of health insurance companies, state administration and tax advisors. Participants will gain a basic overview of medical device price regulation as well as related VAT issues.
  • 06 Mar 2025, 09:30 – 12:00
    Online: Cisco Webex
    The webinar is intended for manufacturers and suppliers who are actively addressing the issue of medical device labelling. The aim of the webinar is not only to offer an overview of the basic labelling rules, but also to focus on updated requirements, especially in the area of UDI labelling.
  • 19 Feb 2025, 09:30 – 12:00
    Online: Cisco Webex
    This webinar is designed primarily for hospital purchasers and staff who administer procurement of medical devices. Participants will gain a detailed overview of medical device regulation, common mistakes, and examples of good practice.
  • 13 Feb 2025, 09:30 – 12:00
    Online: Cisco Webex
    The webinar is intended for medical device manufacturers who need to obtain sufficient clinical evidence for a clinical trial or an update. The seminar is also intended for anyone developing a new medical device who finds clinical trials an organisational and financial barrier difficult to overcome.
  • 12 Feb 2025, 13:00 – 15:30
    Online: Cisco Webex
    The webinar will focus on the topic of clinical trials from the perspective of healthcare providers. The issue of so-called other clinical trials under the MDR will be explained in detail and the related opportunities and limitations of clinical research on or with medical devices will be discussed.
  • 04 Feb 2025, 13:30 – 16:00
    Online: Cisco Webex
    The webinar focuses on the specific requirements of MDR and IVDR for QMS of medical device manufacturers. The seminar is intended for personnel responsible for the implementation of an effective QMS according to the requirements of both EU regulations.
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