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 […]
MDCG Guidance 2024-14 on the implementation of the Master UDI-DI solution for contact lenses has been published this week. By November 2025, manufacturers of standard and […]