Skip to main content
PolicySpeak
← All files
BSF

Bayerisches Staatsministerium für Umwelt und Verbraucherschutz

Public authority · Germany

2
positions filed
in the 326 files tracked
1
legislative file
of 326 tracked
0
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 Bayerisches in PolicySpeak: request access →

Work at Bayerisches Staatsministerium für Umwelt und Verbraucherschutz? so we know who speaks for it.

Follow the file Bayerisches Staatsministerium für Umwelt und Verbraucherschutz engages with

One email on Tuesdays when a new position is filed on this file, from Bayerisches Staatsministerium für Umwelt und Verbraucherschutz or from anyone else on it. 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

Bayerisches Staatsministerium für Umwelt und Verbraucherschutz filed 2 positions between 26 Sept 2025 and 9 Feb 2026, across 1 of the 326 legislative files tracked here.

2025 · 1 filed2026 · 1 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 9 Feb 2026source

As in previous rounds of consultations, the Bavarian State Ministry for the Environment and Consumer Protection welcomes the revision of the EU Regulations on medical devices and in vitro diagnostic medical devices. Many of the known solutions proposed by Bavaria have been implemented by means of this proposal for a Regulation. In our view, however, the requirements for classifying software are not sufficient.

Filed in German · English published by the European Commission

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 26 Sept 2025source

The Bavarian Ministry of the Environment and Consumer Protection continues to welcome the evaluation and revision of the existing EU rules on medical devices (MDRs) and in vitro diagnostic medical devices (IVDRs) to ensure that only safe and effective devices are on the EU market. The objective of increasing patient safety and ensuring a high level of health protection is fully shared.

Filed in German · English published by the European Commission

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

Is this your organization?

Everything on this page comes from Bayerisches Staatsministerium für Umwelt und Verbraucherschutz’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.