🇨🇿 A New Era in Advertising for Medical Devices and In Vitro Diagnostics: A Practical Guide to the Amendment
The proposed amendment to the Regulation of Advertising fundamentally revises the rules governing the advertising of medical devices: it changes the target audience, the mandatory content, specific prohibitions, and establishes new consumer communication rules with , patients and MD professionals.


Date
26 Nov 2026, 09:30 – 12:00
Online: Cisco Webex
About
The event is held in Czech language only!
Current legislation distinguishes primarily between advertising intended for the general public and advertising targeted at professionals and employees of healthcare providers. The proposed amendment fully replaces this concept: it introduces new categories of target audiences, including consumers, patients, and medical device professionals, and lays down certain content requirements and prohibitions on a common basis, regardless of the intended audience.
At the same time, the proposal opens up the possibility of promoting certain medical devices that currently cannot be advertised to the general public, and replaces blanket bans with specific information requirements and warnings. It also sets out a new legal framework for patient and educational programmes.
The webinar will provide a clear comparison of the current and proposed rules and will focus on the practical implications for marketing, sales, patient communication, and internal compliance.
Who is the webinar for:
Medical device manufacturers
Importers and distributors of medical devices
Healthcare providers and staff responsible for purchasing medical devices
Medical device dispensing outlets, pharmacies, online shops, and other retailers of medical devices
Marketing, sales, regulatory, legal, and compliance teams
Advertising agencies and others who create or distribute advertisements for medical devices
Speakers:
JUDr. Jakub Král, Ph.D.
Mgr. Aneta Dostálová
Content:
The background to the amendment to the Act on the Regulation of Advertising, the legislative status of Chamber of Deputies Bill No. 153, and the proposed effective date
New categories of advertising audiences: consumers, patients, and medical device professionals
who will be considered a medical device professional, including persons responsible for servicing and purchasing medical devices for healthcare providers
Changes to the current distinction between advertising aimed at the general public and advertising aimed at professionals
Rules governing advertising for medical devices intended solely for healthcare professionals or dispensed only on prescription
Content-related prohibitions and problematic advertising claims: guarantees of efficacy, comparisons, recommendations by experts and well-known individuals, clinical investigations, patient stories, and natural origin
Comparative advertising, reminder advertising, and advertising intended for consumers and patients
Gifts and other benefits, free samples, hospitality, professional meetings, conferences, and sponsorship
Liability of the advertiser, the advertising producer, and the disseminator; regulatory supervision and the risk of sanctions
Further information:
Participants will have the opportunity to ask questions during the webinar
Each participant will receive a certificate of participation
A PDF presentation will be sent to all participants
Participation fee:
3.900 CZK excluding VAT
100 % cancellation fee applies after bindingly confirmed registration, but with the possibility of sending a replacement participant
Webinar organized by:
Porta Medica Legal s.r.o., advokátní kancelář
IČ: 17491681, DIČ: CZ17491681
Registered office at Opletalova 1525/39, 110 00, Prague 1 - Nové Město