The evaluation of the MDR identified several structural shortcomings affecting the efficiency, predictability, and proportionality of the system, with direct consequences for innovation, device availability, healthcare delivery, and patient access across the Union.
EuromContact
Industry association · Belgium · EU Transparency Register 97208951315-46
Counts here are a floor, never a total: they cover the 665 consultation files tracked so far (57,774 submissions, mostly 2021–26), so an organization's real filing history is larger, not smaller.
Who they are
Among the 1518 trade and business associations on this site, they rank #543 by legislative files engaged, a count of participation, not a measure of influence.
Declares membership of
- Euromcontact is a member of the ad hoc Platform European Coalition for vision, a Platform comprising industry, health…
Self-declared to the EU Transparency Register (snapshot 14 Oct 2026).
- Register category
- Trade and business associations
- Registered as
- EUROMCONTACT
- Head office
- Bruxelles, Belgium
Self-declared to the EU Transparency Register (snapshot 14 Oct 2026); cost bands are floors, not audited totals. Reused under Commission Decision 2011/833/EU.
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Their record over time
EuromContact filed 7 positions between 25 May 2021 and 3 Jun 2026, across 6 of the 665 legislative files tracked here, attaching a full position paper 6 times.
What they argued
EuromContact, representing manufacturers of contact lenses and lens care products, welcomes the targeted revision of the MDR and its objectives to streamline and future-proof the regulatory framework by reducing the administrative burden and enhancing predictability and cost-efficiency, while preserving a high level of public health and patient safety.
EuromContact strongly supports the general objective for the revision of Directive 94/62/EC on Packaging and Packaging Waste to transform it into a regulation and tackle the environmental impact of packaging and packaging waste. The contact lens and lens care manufacturers have substantially minimized the packaging for their products.
EuromContact agrees with the initial postulate of the proposal : many devices which may be placed on the market in accordance with the initial MDR transitional provisions are not going to be certified in accordance with that Regulation before the end of the transition period, which leads to a major risk of shortages of medical devices in the EU.
The European association representing manufacturers of contact lenses and lens care products, EuromContact, welcomes the opportunity to comment on the draft Commission implementing regulation developed under Article 24 of the Ecodesign for Sustainable Products Regulation (ESPR).
EuromContact, the European association representing manufacturers of contact lenses and lens care products, welcomes this consultation and agrees with the assessment that MDR implementation has shown inconsistent and divergent interpretations of certain requirements set out in MDR Annex VII, especially as regards the timelines for completing conformity assessment activities and re-certification.
EUROMCONTACT is the association representing the contact lens and lens care products manufacturers in the European Union. We represent more than 90% of the soft contact lens and 80% of the contact lens care products, and more than 50% of the rigid contact lenses in the European market.
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Turns up on the same files
Organizations that also filed on at least two of the same consultations. A shared interest in the same dossiers, not evidence of coordination, and we do not suggest any.
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Everything on this page comes from EuromContact’s own submissions to the European Commission. We have added nothing and interpreted nothing. If something is wrong or out of date, email info@policyspeak.com and we will correct it. If you are an individual named in a record, our privacy policy sets out your rights to correction, objection and removal.
Quotes are verbatim from submissions published by the European Commission, trimmed to their opening passage and never summarized by a model. Organizations only, never individuals. Reused under Commission Decision 2011/833/EU; the European Commission is not liable for this reuse.