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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

April 2025
Mon
Tue
Wed
Thu
Fri
Sat
Sun
31
1
9:30
🇨🇿 Obligations of importers and distributors of medical devices - good practice and news
+1 more
2
3
4
5
6
7
8
9
9:30
🇨🇿 Overview of new developments in the regulation of medical devices and IVDs
+1 more
10
11
12
13
14
15
9:30
🇨🇿 Getting ZUM reimbursement step by step
+1 more
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
1
2
3
4
5
6
9:30
🇨🇿 How to successfully prepare a public tender for a medical device
+1 more
7
8
9
10
11

Past Events

  • 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.
  • 19 Dec 2024, 09:30 – 12:00
    Online: Cisco Webex
    The last in a series of three webinars on risk management according to EN ISO 14971:2020 and ISO/TR 24971:2020, intended mainly for manufacturers of medical devices. This is an updated repeat of the successful online seminars held in 2023.
  • 11 Dec 2024, 09:30 – 12:30
    Online: Cisco Webex
    The webinar is designed for manufacturers who have launched their devices under previous legislation, are awaiting their first MDR certification and are unsure whether their clinical evaluation will be sufficient.
  • 05 Dec 2024, 09:30 – 12:00
    Online: Cisco Webex
    The second of three webinars on risk management according to EN ISO 14971:2020 and ISO/TR 24971:2020, intended mainly for medical device manufacturers. This is an updated repeat of the successful online seminars held in 2023.
  • 21 Nov 2024, 09:30 – 12:00
    Online: Cisco Webex
    The first of three webinars on risk management according to EN ISO 14971:2020 and ISO/TR 24971:2020, designed especially for medical device manufacturers. This is an updated repeat of the successful online seminars held in 2023.
  • 19 Nov 2024, 09:30 – 12:00
    Online: Cisco Webex
    The webinar focuses on the rules of advertising of medical devices and IVDs from the perspective of European and Czech law. You will learn how advertising to professionals differs from advertising to the general public and we will introduce you to the changes that are coming in this area.
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