Skip to main content
PolicySpeak
← All files
RI

Regulatory Institute

NGO · Belgium

4
positions filed
in the 326 files tracked
4
legislative files
of 326 tracked
1
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 Regulatory in PolicySpeak: request access →

Work at Regulatory Institute? so we know who speaks for it.

Follow the files Regulatory Institute engages with

One email on Tuesdays when a new position is filed on these 4 files, from Regulatory Institute 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

Regulatory Institute filed 4 positions between 30 Sept 2025 and 3 Mar 2026, across 4 of the 326 legislative files tracked here, attaching a full position paper 1 time.

2025 · 1 filed2026 · 3 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 30 Sept 2025source

We are pleased to submit our response to the Call for Evidence on the targeted revision of the EU rules for medical devices and in vitro diagnostics. In terms of potential simplification and burden reduction for economic operators, we recommend continuing the approach taken for decades by EU medical devices legislation: integrating substantial requirements from other EU legislation to avoid double certification.

Revision of EU rules on public procurementfiled 22 Jan 2026source

The Regulatory Institute is pleased to share its EU Legislators' Toolbox. The toolbox contains over 340 tools designed and actually used to strengthen EU regulatory systems and standardise their implementation. It draws on knowledge from many different regulatory sectors. Reference wordings can be found in the references cited in the toolbox and the attached document.

Evaluation of the Biocidal Products Regulationfiled 3 Mar 2026PDFsource

Regulatory Institute Response to the Call for Evidence on Biocidal Products Regulation – Evaluation www.howtoregulate.org The Regulatory Institute is pleased to submit its response to the Call for Evidence on the Biocidal Products Regulation – Evaluation. The Regulatory Institute is a non-profit think tank committed to improving regulation globally so that regulations benefit us all.

Opening of the attached position paper · the full paper is on the Commission’s record (source link above)

EU Strategy on Combating Trafficking in Human Beings 2026-2030filed 22 Jan 2026source

The Regulatory Institute is pleased to submit its feedback on the EU strategy on combating trafficking in human beings 2026-2030. The Regulatory Institute is a non-profit think tank dedicated to improving regulation globally so that regulations benefit us all.

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 27.

Is this your organization?

Everything on this page comes from Regulatory Institute’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.