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GIR

GIRP

Industry association · Belgium · EU Transparency Register 0757172464-29

2
positions filed
in the 326 files tracked
2
legislative files
of 326 tracked
2
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.

Who they are

Among the 1205 trade and business associations on this site, they rank #743 by legislative files engaged — a count of participation, not a measure of influence.

11
declared lobbying FTE
self-declared
€50K+
declared costs / yr (floor)
4
EP accreditations
as declared to the register
2008
in the register since

Declares membership of

  • Membership:
  • EMVO (European Medicines Verification Organisation)
  • IFPW (International Federation of Pharmaceutical Wholesalers)
  • EuroCommerce
  • Relation with other Bodies:
  • WHO
  • COE (Export Group on Counterfeit Medicines)
  • EMA
  • CMA
  • Networks:
  • AESGP
  • EFPIA
  • and 10 more

Self-declared to the EU Transparency Register (snapshot 30 Aug 2026).

Register category
Trade and business associations
Registered as
European Healthcare Distribution Association (GIRP)
Head office
Brussels, Belgium

Self-declared to the EU Transparency Register (snapshot 30 Aug 2026); cost bands are floors, not audited totals. Reused under Commission Decision 2011/833/EU.

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Follow the files GIRP engages with

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Their record over time

GIRP filed 2 positions between 8 Sept 2025 and 6 Oct 2025, across 2 of the 326 legislative files tracked here, attaching a full position paper 2 times.

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 6 Oct 2025PDFsource

GIRP, the European Healthcare Distribution Association, welcomes the opportunity to contribute to the European Commissions Call for Evidence on the targeted revision of the EU rules for medical devices and in vitro diagnostics.

Clean corporate vehiclesfiled 8 Sept 2025PDFsource

GIRP, the European Healthcare Distribution Association welcomes the opportunity given by the Commission to give feedback on the Regulation on Clean Corporate Vehicles. GIRP represents the national associations of over 500 pharmaceutical full-line wholesalers operating across 33 European countries, alongside major pan-European and international healthcare distribution companies.

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 7.

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Everything on this page comes from GIRP’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.