Counts here are a floor, never a total: they cover the 326 consultation files tracked so far (29,503 submissions, mostly 2025–26), so an organization's real filing history is larger, not smaller.
Work at Pro-PLUS S.A.? so we know who speaks for it.
Their record over time
Pro-PLUS S.A. filed 2 positions between 3 Oct 2025 and 8 Jan 2026, across 2 of the 326 legislative files tracked here, attaching a full position paper 1 time.
I am a representative of a small company which produces medical devices in a technology known for many years, has been developed in the course of implementing the requirements of the MDD Directive into Polish regulations and is still being implemented under the MDR transitional period, with minor changes.
Filed in Polish · English published by the European Commission
The proposed changes address only part of the problems related to the functioning of notified bodies that medical device manufacturers face in practice. In particular, they do not resolve key issues concerning costs, timeliness of activities, and contractual relationships.
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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.
Everything on this page comes from Pro-PLUS S.A.’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 If something is wrong or out of date, email info@policyspeak.com and we will correct it.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.