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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
- 🇨🇿 How to successfully prepare a public tender for a medical device06 May 2025, 09:30 – 12:00Online: Cisco Webex
Calendar
April 2025
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9:30
🇨🇿 Obligations of importers and distributors of medical devices - good practice and news
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9:30
🇨🇿 Overview of new developments in the regulation of medical devices and IVDs
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9:30
🇨🇿 Getting ZUM reimbursement step by step
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9:30
🇨🇿 How to successfully prepare a public tender for a medical device
+1 more
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Past Events
- Tue 15 Apr15 Apr 2025, 09:30 – 12:00Kancelář Porta Medica, Opletalova 1525/39, Nové Město, 110 00 Praha-Praha 1, CzechiaA 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.
- Wed 09 Apr09 Apr 2025, 09:30 – 12:00Online: Cisco WebexThis 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.
- Tue 01 Apr🇨🇿 Obligations of importers and distributors of medical devices - good practice and news /Online: Cisco Webex01 Apr 2025, 09:30 – 12:00Online: Cisco WebexA 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.
- Wed 19 Mar19 Mar 2025, 08:30 – 11:30Online: Cisco WebexAn 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.
- Tue 11 Mar11 Mar 2025, 09:30 – 12:00Online: Cisco WebexThe 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.
- Thu 06 Mar06 Mar 2025, 09:30 – 12:00Online: Cisco WebexThe 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.
- Wed 19 Feb
- Thu 13 Feb13 Feb 2025, 09:30 – 12:00Online: Cisco WebexThe 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.
- Wed 12 Feb12 Feb 2025, 13:00 – 15:30Online: Cisco WebexThe 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.
- Tue 04 Feb
- Thu 19 Dec🇨🇿 Risk Management III – The Most Difficult Parts of Risk Management in MDR and IVDR /Online: Cisco Webex
- Wed 11 Dec
- Thu 05 Dec
- Thu 21 Nov
- Tue 19 Nov19 Nov 2024, 09:30 – 12:00Online: Cisco WebexThe 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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