Skip to main content
PolicySpeak
← All files
GEH

GIRP - European Healthcare Distribution Association

Industry association · Belgium · EU Transparency Register 0757172464-29

7
positions filed
in the 665 files tracked
6
legislative files
of 665 tracked
5
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.

Who they are

Among the 1518 trade and business associations on this site, they rank #551 by legislative files engaged, a count of participation, not a measure of influence.

11
declared lobbying FTE
self-declared
€50K+
declared costs / yr (floor)
8
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 14 Oct 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 14 Oct 2026); cost bands are floors, not audited totals. Reused under Commission Decision 2011/833/EU.

Track GIRP in PolicySpeak: request access →

Follow GIRP - European Healthcare Distribution Association

An email when this organization files on a consultation we publish.

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

Work at GIRP - European Healthcare Distribution Association? so we know who speaks for it.

Their record over time

GIRP - European Healthcare Distribution Association filed 7 positions between 2 Feb 2021 and 6 Oct 2025, across 6 of the 665 legislative files tracked here, attaching a full position paper 5 times.

2021 · 3 filed2022 · 1 filed2023 · 1 filed2025 · 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 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.

Medicinal products for human usefiled 8 Nov 2023PDFsource

Please find attached GIRP's contribution to the European Commissions public consultation on the Revision of the EU general pharmaceuticals legislation. GIRP, the European Healthcare Distribution Association, welcomes the revision of the EU General Pharmaceutical Legislation and the opportunity to provide feedback to the European Commission on the published text.

Medicinal products for human usefiled 27 Apr 2021PDFsource

GIRP welcomes the opportunity to comment on the evaluation and revision of the general pharmaceutical legislation by the European Commission (EC). GIRP identifies 4 key areas to improve access to medicines: 1. Ensure through a regulated and enforced framework (with appropriate incentives) the safe, efficient, and fair distribution of medicinal products, and medical devices, to all patients in crisis and non-crisis…

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.

Resilience of critical entitiesfiled 8 Apr 2021source

GIRP welcomes the Proposal for a directive of the European Parliament and of the Council on the resilience of critical entities and the harmonisation purpose it serves to apply a uniform approach in identifying critical entities, while also accounting for specificities at national level, including varying levels of risk exposure and interdependencies between sectors and over borders.

European Medicines Agencyfiled 2 Feb 2021PDFsource

GIRP welcomes the proposed regulation on a reinforced role for the EMA in crisis preparedness and management for medicinal products and medical devices. GIRP believes that EU coordination is key to addressing the issue of medicine shortages in times of crisis and we are convinced that the EMA is well-fitted to monitor and mitigate potential and actual shortages for the duration of a public health emergency or major…

Single Market emergency instrumentfiled 11 May 2022source

GIRP welcomes the initiative of the European Commission to adopt legislative and non-legislative measures to implement a flexible and transparent mechanism to strengthen the resilience of the European single market. As a cornerstone of the European Union, the Single Market and the freedom of movements of goods is a key component of the ever closer Union that impregnates the spirit of the Treaties.

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

Put GIRP - European Healthcare Distribution Association next to another organization. Same files, same register facts, side by side. Compare →

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 73.

Is this your organization?

Everything on this page comes from GIRP - European Healthcare Distribution Association’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.