News

On 16 December 2025, the European Commission proposed a targeted revision of the Regulation (EU) 2017/745 on medical devices (MDR) with the objective of addressing key […]

EuromContact has published its annual syndicated market data report for 2025, revealing solid growth in 2025, reaching a total value of €2.5 billion at industry level […]

On April 13, EuromContact hosted an online workshop entitled “Getting ready for EUDAMED and Swissdamed compliance – Device registration for contact lenses and lens care products.” […]

EuromContact has submitted its contribution to the public consultation launched by the Medicines and Healthcare products Regulatory Agency (MHRA) on the indefinite recognition of CE-marked medical […]

EuromContact has updated its factsheet to assist Eye Care Professionals (ECPs) to familiarize themselves with the Unique Device Identifier (UDI) system created by the Medical Devices […]

EuromContact commissioned Anthesis, a sustainability consultancy, to develop a consistent methodology for assessing the environmental impacts of soft and rigid contact lenses as well as lens care […]

In June 2025, the electronic instructions for use (eIFU) regulation (EU Regulation 2021/2226) has been updated, expanding the possibility of eIFU to all professional use devices. […]

With the ongoing targeted evaluation of the MDR, EuromContact has conducted a comprehensive review of the EU Medical Devices Regulation (MDR) to assess its impact and identify […]

During its first meeting of the year, the EuromContact Board reviewed recent activities and set key priorities for the year ahead. The Board also elected its […]