CONGRESS

2026

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Press registration

EADV welcomes the interest of the press and media about the EADV Congress 2026 in vIENNA.

Here you can register as press and find out further information about press and media activities at the Congress.

INFORMATION ABOUT THE EADV CONGRESS 2026 WILL BE PUBLISHED SOON

Register now
Social Media toolkit

How to register as a press representative

Log in or sign up for the EADV Congress Registration Platform and click on the Application Module.

Press registration is available until Wednesday, 3 Sept 2025 (23:59 CEST).

Applications

See the available applications

Register now

Access type

Press Ticket

  • The Press Ticket includes:
  • Name badge
  • Admission to live Congress Scientific Sessions
  • Admission to the Networking Symposium on Wednesday 17 September 2025 (No entertainment)
  • Access to Subspecialty sessions
  • Access to ePosters area, MyEADV Booth and Patient Organisations Area
  • Access to the Exhibition hall  (for Specialised Press only)
  • Access to Satellite Symposia Sessions *  (for Specialised Press only)
  • Access to the live-streaming of selected Satellite Symposia and Industry Expert Hub sessions *
  • Transportation pass

Along with the virtual access

Virtual access

  • The virtual access includes:
  • Access to the virtual Congress Platform with live-streamed scientific sessions
  • Access to all on-demand content until 31 December 2025
  • Access to the streaming of Subspecialty sessions
  • Access to the online library of ePosters and abstracts
  • Access to the online EADV area and Patient Organisations Area
  • Access to exhibiting company profiles (for Specialised Press only)
  • Access to the live-streaming of selected Satellite Symposia and Industry Expert Hub sessions *

Access to the EADV Congress 2025 is granted to members of the medical and professional media. However, relevant representatives of consumer media who require access will be considered on a case-by-case basis.

* Industry is allowed to restrict press access to their Industry Satellite Sessions

Terms and conditions for press registration

  • The free registration under the Press/Media Representative category is granted only to journalists or media representatives in possession of:
    • A valid press card or an appropriate letter of assignment
    • A completed EADV Press and Media Representatives Online Application
  • To secure your access to the start of the Congress, registration is required by Wednesday, 3 September 2025 (23:59 CEST). After this date, EADV cannot guarantee that your application will be processed before the Congress begins.
  • Onsite registration will not be possible. 
  • Press Registration includes access to all EADV scientific sessions, interviews with EADV spokespersons, and more.

Exhibition & HCP restricted sessions

Journalists from specialised press covering the event for healthcare professionals may be exposed to advertising for prescription-only medicinal products. This does not apply to regular press serving the general public or specialised press targeting non-healthcare professionals. For this reason, the Exhibition Area has restricted access: 

Regular Press

  • Access to all EADV scientific sessions
  • Access to Industry Satellite Session(s) (if open to Non HCPs)
    The organising company may restrict press access to their session.

Regular press do not have access to the Exhibition Area.

Specialised Press

  • Access to all EADV scientific sessions
  • Access to the EADV Exhibition Area
  • Access to Industry Satellite Session(s)
    The organising company may restrict press access to their session.

It is the responsibility of each press representative to ensure that the information submitted via the Press Representative online application is accurate and true.

Media & Embargo Policy

EADV Congress 2025

Media Partners

EMJ Dermatology
Umer Doctor

Healthcare Professional definition

  1. Important note to Healthcare and Non-Healthcare Professionals

    Access to the different areas and sessions of the Congress depends on Healthcare Professional status.

    As a multidisciplinary audience will attend the EADV Congress, the EADV will assign different classes to Healthcare Professionals (HCPs) and Non-Healthcare Professionals (non-HCPs) to ensure compliance with the Austrian Pharmaceutical industry (PHARMIG) Code of Conduct and the medical device industry code of conduct (AUSTROMED) (Kodex und Statuten der AUSTROMED – Erklärvideo).

    Please read the description below to ensure that you (or your delegates) comply with the regulations in place.

EADV members are not automatically considered Healthcare Professionals

Please select the correct status (HCP or non-HCP) during registration.

  1. Definition

    The PHARMIG code defines Healthcare Professionals as follows (art. 2.2):

    “Healthcare Professional:

     “…any natural person(s) authorized to administer, to dispense, and to prescribe medicinal products such as doctors, pharmacists, dental practitioners, veterinarians, dentists, midwives, nursing professionals, medical technicians, medical service professionals, and other medical services organizations, provided that such medicinal products are necessary for the discharge of their duties.”

    Medical students are not considered Healthcare Professionals under the current guidelines and will be automatically classified as Non-Healthcare Professionals
  1. Industry sessions

    Satellite Symposia and Industry Hub Sessions presenting data on the development, research, or other issues related to prescription medicine is restricted to Healthcare Professionals and Non Member (INDUSTRY) as indicated by the Industry Session Organizer.

    All promotional materials and marketing aids related to these industry sessions should be strictly limited to HCPs.

    Industry Session organisers can limit participation to certain representative groups independently from the EADV recommendations if deemed imperative to achieving the session’s intended purpose. The organising company reserves the right to refuse single categories, particularly if they are not adequately related to the session’s objective and purpose.

    The industry session organiser is responsible for compliance with the session.