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The Association of Manufacturers and Suppliers of Medical Devices (AVDZP)

Industry association · Czechia

not in the EU Transparency RegisterThis organization files on consultations without a register number, so its record here is built from its filings alone. Register facts (staff, costs, accreditations) are not available for it.

3
positions filed
in the 665 files tracked
2
legislative files
of 665 tracked
3
with a full position paper
attached to a submission

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.

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Their record over time

The Association of Manufacturers and Suppliers of Medical Devices (AVDZP) filed 3 positions between 6 Oct 2025 and 3 Aug 2026, across 2 of the 665 legislative files tracked here, attaching a full position paper 3 times.

2025 · 1 filed2026 · 2 filed

What they argued

Simplifying and reducing the burden of the rules on medical devices and in vitro diagnostic medical devices, and support of the European Medicines Agency for the expert panels on medical devices and the list of Union harmonisation legislationfiled 3 Aug 2026PDFsource

AVDZP Association of Manufacturers and Suppliers of Medical Devices (Czech Republic) welcomes the targeted revision COM(2025) 1023 and its aim to simplify the framework, reduce administrative burden and support timely patient access to innovation, while preserving safety. A detailed position paper covering 30 priority areas is attached; the key points are summarised below.

Simplifying and reducing the burden of the rules on medical devices and in vitro diagnostic medical devices, and support of the European Medicines Agency for the expert panels on medical devices and the list of Union harmonisation legislationfiled 6 Oct 2025PDFsource

The Association of Manufacturers and Suppliers of Medical Devices (AVDZP), representing the Czech MedTech industry across the full value chain, welcomes the opportunity to contribute to the targeted revision of Regulation (EU) 2017/745 (MDR).

Implementing rules regarding requirements to be met by notified bodiesfiled 23 Jan 2026PDFsource

The Association of Manufacturers and Suppliers of Medical Devices (AVDZP), representing the Czech MedTech industry across the full value chain, welcomes the European Commissions initiative on the uniform application of requirements for notified bodies (Implementing Regulation draft, Ares(2025)11081575). Please find attached AVDZPs feedback.

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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.

Showing 5 of 26.

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Everything on this page comes from The Association of Manufacturers and Suppliers of Medical Devices (AVDZP)’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.