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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

  • Thu 26 Mar
    Online: Cisco Webex
    26 Mar 2026, 09:30 – 12:00
    Online: Cisco Webex
    The rules for "in-house" manufacturing have changed fundamentally under pressure from the MDR and IVDR regulations, and another wave of legislative changes is on it way. Don't wait for the changes to resolve the situation for you and find out in time how to keep your operations in compliance.
  • Wed 25 Mar
    Online: Cisco Webex
    25 Mar 2026, 09:30 – 12:00
    Online: Cisco Webex
    Few companies can boast that they perform all activities related to the life cycles of medical devices and in vitro diagnostic medical devices internally. In our webinar, we will look at how to set up these activities through other parties correctly so that they are not just a formal burden.
  • Wed 11 Mar
    Online: Cisco Webex
    11 Mar 2026, 09:30 – 12:00
    Online: Cisco Webex
    Intended for all suppliers of medical devices who consider including their products in the public health insurance reimbursement system. This webinar aims to clarify basic concepts in the areas of prices and reimbursements of prescription medical devices, including less common mechanisms such as DNC
  • Wed 04 Mar
    Online: Cisco Webex
    04 Mar 2026, 09:30 – 12:00
    Online: Cisco Webex
    Online seminar designed for hospital purchasers, lawyers, and managers involved in the procurement of medical devices. The seminar will offer a practical look at how to balance the requirements for transparent and efficient purchasing with specific regulations governing medical devices and more.
  • Tue 24 Feb
    Online: Cisco Webex
    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.
  • Thu 12 Feb
    Online: Cisco Webex
    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.
  • Tue 03 Feb
    Online: Cisco Webex
    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.
  • Wed 28 Jan
    Online: Cisco Webex
    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.
  • Tue 27 Jan
    Online: Cisco Webex
    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.
  • Wed 10 Dec
    Online: Cisco Webex
    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.
  • Wed 03 Dec
    Online: Cisco Webex
    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.
  • Tue 02 Dec
    Grandium Hotel Prague
    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.
  • 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.
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