top of page

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

December 2025
Mon
Tue
Wed
Thu
Fri
Sat
Sun
1
2
9:30
🇨🇿 Annual Conference MEDICAL DEVICES 2025
+1 more
3
9:30
🇨🇿 UDI and medical device labeling – news and practical experience
+1 more
4
5
6
7
8
9
10
9:30
🇨🇿 Mandatory ePrescription and the issue of dispensing medical devices in doctors' offices
+1 more
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
1
2
3
4
5
6
7
8
9
10
11

Past Events

  • Wed 26 Nov
    Online: Cisco Webex
    26 Nov 2025, 13:00 – 15:30
    Online: Cisco Webex
    The aim of the seminar is to prepare custom device manufacturers to optimally meet the requirements of the MDR and Act No. 375/2022 Sb. The program will also include practical advice and recommendations based on the inspection practices of the State Institute for Drug Control.
  • Wed 19 Nov
    Online: Cisco Webex
    19 Nov 2025, 09:30 – 12:00
    Online: Cisco Webex
    We invite you to a webinar focused on preparing entities operating in the field of medical devices and IVDs for inspections of the State Institute for Drug Control (SÚKL). The aim of the webinar is to present the procedural framework of the inspection, its course and specifics concerning subjects.
  • Thu 13 Nov
    Online: Cisco Webex
    13 Nov 2025, 09:30 – 12:00
    Online: Cisco Webex
    Join our online seminar designed for anyone considering conducting a clinical trial or, conversely, looking for ways to avoid clinical trials. The issue of clinical trials will be explained in the context of the manufacturer's obligations to demonstrate compliance with clinical safety and efficacy.
  • Tue 11 Nov
    Online: Cisco Webex
    11 Nov 2025, 09:30 – 12:00
    Online: Cisco Webex
    A webinar for all medical device suppliers who are considering adding their products (ZUM) – to the VZP-ZP Reimbursement Catalog. Participants will gain an overview of the procedure, key documentation requirements, and practical steps for successfully submitting a proposal.
  • Wed 05 Nov
    Online: Cisco Webex
    05 Nov 2025, 09:30 – 12:00
    Online: Cisco Webex
    The webinar is intended for medical and non-medical staff who handle medical devices, especially those responsible for the management or purchase of medical devices. The aim of the webinar is to introduce participants to the practical use of the EUDAMED database in healthcare facilities.
  • Thu 30 Oct
    Online: Cisco Webex
    30 Oct 2025, 09:30 – 12:00
    Online: Cisco Webex
    During the seminar, participants will be introduced to the key legislative obligations related to the EUDAMED database. Updates will be presented on the latest developments on deadlines and registration methods for all types of medical devices.
  • Thu 16 Oct
    Online: Cisco Webex
    16 Oct 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.
  • Thu 09 Oct
    Grandium Hotel Prague
    09 Oct 2025, 15:00 – 18:00
    Grandium Hotel Prague, Politických vězňů 913/12, Nové Město, 110 00, Prague 1, Czechia
    An informal platform for regulated entities to meet with representatives of key institutions in the healthcare sector, as well as current and former politicians who have insight into the regulation of medical devices. The event is intended for everybody who deals with medical devices.
  • Thu 09 Oct
    Online: Cisco Webex
    09 Oct 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.
  • Fri 26 Sept
    Europe
    26 Sept 2025, 00:00
    Europe
    Deadline to sign a written agreement with a notified body for IVDs that would become Class D under IVDR in order to benefit from extended transition period.
  • Fri 26 Sept
    Europe
    26 Sept 2025, 00:00
    Europe
    Deadline to transfer appropriate surveillance to an IVDR notified body for all IVDs in order to benefit from extended transition period.
  • Thu 18 Sept
    Online: Cisco Webex
    18 Sept 2025, 13:00 – 15:30
    Online: Cisco Webex
    The webinar is intended for healthcare providers in the field of aesthetic medicine and anyone who manufactures or plans to manufacture products without therapeutic purposes. It is also intended for distributors and importers of these products.
  • Wed 17 Sept
    Online: Cisco Webex
    17 Sept 2025, 09:30 – 12:00
    Online: Cisco Webex
    An online webinar that will focus on good practice in the handling of medical devices and in-vitro diagnostic medical devices in the hospital environment. The webinar will provide an overview of current legislative requirements, highlight the most common problem areas and offer practical solutions.
  • Tue 16 Sept
    Online: Cisco Webex
    16 Sept 2025, 09:30 – 12:00
    Online: Cisco Webex
    Do you want to minimize the risk of unexpected findings during your next audit? Join the online seminar for medical device manufacturers and gain practical know-how to successfully prepare for an audit from a notified body.
  • Tue 09 Sept
    Online: Cisco Webex
    09 Sept 2025, 09:30 – 12:00
    Online: Cisco Webex
    The online seminar is designed for medical device manufacturers and contract manufacturers outsourcing manufacturing activities. The webinar will explain the complex requirements of MDR/IVDR and, in their context, the benefits and shortcomings of using the harmonized standard EN ISO 13485.
bottom of page