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AbbVie

Company · Belgium · EU Transparency Register 934069612666-51

4
positions filed
in the 665 files tracked
4
legislative files
of 665 tracked
1
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 (57,800 submissions, mostly 2021–26), so an organization's real filing history is larger, not smaller.

Who they are

Among the 1212 companies & groups on this site, they rank #375 by legislative files engaged, a count of participation, not a measure of influence.

2.5
declared lobbying FTE
self-declared
€1M+
declared costs / yr (floor)
3
EP accreditations
as declared to the register
2014
in the register since

Declares membership of

Self-declared to the EU Transparency Register (snapshot 15 Oct 2026).

Register category
Companies & groups
Head office
North Chicago, United states
EU office
Brussels

Self-declared to the EU Transparency Register (snapshot 15 Oct 2026); cost bands are floors, not audited totals. Reused under Commission Decision 2011/833/EU.

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Their record over time

AbbVie filed 4 positions between 6 Jan 2021 and 3 Aug 2026, across 4 of the 665 legislative files tracked here, attaching a full position paper 1 time.

2021 · 2 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 2026source

AbbVie welcomes the Commissions targeted revision of the MDR/IVDR and appreciates the intent to update Regulation (EU) 2017/745 based on practical experience and broadly supports many of the Commissions proposals. These proposals introduce important measures to support innovation and improve regulatory efficiency, however, there is room for further improvement on several aspects.

Medicinal products for human usefiled 27 Apr 2021source

As a research-driven biopharmaceutical company, AbbVie supports the Commission objectives to create a patient-centered and globally competitive European pharmaceutical policy environment that enhances the availability of medicines across the EU and incentivizes development of treatments for unmet health needs in both diseases where no treatments exist as well as those where the existing treatments do not…

Revision of the EU legislation on medicines for children and rare diseasesfiled 6 Jan 2021source

As an innovative biopharmaceutical company with over 11.000 employees in the EU, AbbVie supports the Commission’s aims to develop more medicines for unmet needs, speed access to new therapies for all EU citizens, and ensure the maximum benefits from scientific and technological advances.

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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 109.

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Everything on this page comes from AbbVie’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.