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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

Past Events

  • 24 Feb 2026, 09:30 – 12:00
    Online: Cisco Webex
    The webinar focuses on practical execution of literature review in the context of current regulatory requirements according to recommendatory documents and on the correct integration of the review with the clinical evaluation of the medical device as well as creation of Literature Search Protocol.
  • 12 Feb 2026, 09:30 – 12:00
    Online: Cisco Webex
    We invite you to attend a specialist online webinar focusing on the proposed extensive revision of the MDR regulation, as currently presented by the European Commission. The webinar will offer a comprehensive overview of the proposed changes and their practical implications.
  • 03 Feb 2026, 09:30 – 12:00
    Online: Cisco Webex
    For some, it is a feared term with unknown content, representing an imaginary bogeyman to avoid. For others, it is the centerpiece of their work activities, which they are accustomed to working with. Whether you are a beginner or an experienced regulatory expert, our webinar is designed for both.
  • 28 Jan 2026, 09:30 – 12:00
    Online: Cisco Webex
    After recent announcement of the first four modules of the EUDAMED database being fully functional, the date for mandatory use of this database is fast approaching. In our webinar, we will create a practical guide for reliable fulfilment of the essential obligations for relevant economic operators.
  • 27 Jan 2026, 09:30 – 12:00
    Online: Cisco Webex
    Revision ISO 10993-1:2025 changes the way manufacturers approach biocompatibility assessment. Biological safety is no longer just about choosing the right tests. This webinar will present main changes in the new standard and provide a comprehensive insight into current assessment requirements.
  • 10 Dec 2025, 09:30 – 12:00
    Online: Cisco Webex
    This online seminar is primarily intended for prescribers and dispensers of medical devices, but it is also relevant for supplier representatives. The aim of the webinar is to familiarize professionals with fundamental changes that will take effect on January 1, 2026.
  • 03 Dec 2025, 09:30 – 12:00
    Online: Cisco Webex
    The online seminar is intended for manufacturers, distributors, and importers who are actively addressing the issue of medical device labeling. The aim of the seminar is not only to provide an overview of the basic rules of labeling, but also to focus on updated requirements and their refinement.
  • 02 Dec 2025, 09:30 – 16:50
    Grandium Hotel Prague, Politických vězňů 913/12, Nové Město, 110 00 Praha 1, Czechia
    The seventh annual Medical Devices Conference. An all-day event divided into three thematic blocks covering all the key developments in the regulation of medical devices from the perspective of state supervisory authorities, suppliers, health insurance companies, and hospitals.
  • 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.
  • 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
    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.
  • 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.
  • 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.
  • 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.
  • 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.
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