Skip to main content
PolicySpeak
← All files
AMS

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

Industry association · Czechia

3
positions filed
in the 326 files tracked
2
legislative files
of 326 tracked
3
with a full position paper
attached to a submission

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.

Track The in PolicySpeak: request access →

Work at The Association of Manufacturers and Suppliers of Medical Devices (AVDZP)? so we know who speaks for it.

Follow the files The Association of Manufacturers and Suppliers of Medical Devices (AVDZP) engages with

One email on Tuesdays when a new position is filed on these 2 files, from The Association of Manufacturers and Suppliers of Medical Devices (AVDZP) or from anyone else on them. Only when there is something new.

We use your email for these updates, and PolicySpeak may contact you about the product. Unsubscribe in one click. Privacy policy.

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 326 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.

Looking for an argument rather than an organization? Search every submission for a phrase and see everyone who used it.

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.

Is this your organization?

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.