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Novartis

Company · Belgium · EU Transparency Register 91269481588-28

3
positions filed
in the 326 files tracked
3
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.

Who they are

Among the 925 companies & groups on this site, they rank #303 by legislative files engaged — a count of participation, not a measure of influence.

3.2
declared lobbying FTE
self-declared
€2.5M+
declared costs / yr (floor)
6
EP accreditations
as declared to the register
2009
in the register since

Declares membership of

  • Business Europe Membership
  • Critical Medicines Alliance
  • ECPA
  • EFPIA - Pillar 3 IMI
  • EFPIA (Pillar 1+2)
  • EFPIA: Pillar 3 ICH
  • EFPIA Country engagement
  • EFPIA Campaign mode
  • EFPIA - Contribution to Fairer pharmaceutical spending & improved industrial ecosystem in Europe 'advocacy 1 communic…
  • Eucope (Membership)
  • Eucope Membership - Support to the incentive Steering Group (ISG)
  • Eucope Membership (OLU WG)
  • and 19 more

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

Register category
Companies & groups
Registered as
Novartis International AG
Head office
Basel, Switzerland
EU office
Brussels

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 Novartis engages with

One email on Tuesdays when a new position is filed on these 3 files, from Novartis or from anyone else on them. Only when there is something new.

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Their record over time

Novartis filed 3 positions between 24 Apr 2026 and 5 Aug 2026, across 3 of the 326 legislative files tracked here, attaching a full position paper 1 time.

What they argued

European Biotech Actfiled 5 Aug 2026PDFsource

Novartis welcomes the Biotech Act as a concrete step towards strengthening Europes life sciences ecosystem. By promoting simplification, regulatory coherence, reduced administrative burden and a stronger IP framework, the Act can support innovation and enhance Europes attractiveness for research, development, manufacturing and investment. To maximise its impact, Novartis highlights three priorities. 1.

Health Checks for Cardiovascular diseasesfiled 18 May 2026source

Novartis welcomes the European Commissions initiative to strengthen early detection and screening of cardiovascular diseases (CVDs) as a core pillar of the EU Safe Hearts Plan. CVDs remain the leading cause of mortality and morbidity in Europe, requiring more systematic and appropriate CV risk stratification to reduce avoidable disease, health inequalities and long-term pressure on health systems.

Evaluation of Radioactive Waste Directive and Shipment Directivefiled 24 Apr 2026source

Lifesaving nuclear medicine should be regulated with the same rigor as other nuclear activities, but not in the same way. For innovative radiopharmaceuticals, high safety standards can be maintained while reducing unnecessary system burden by applying a pragmatic, risk and exposure-based approach to radioactive waste management, grounded in low medical doses, low volumes, safe handling conditions, and real-world…

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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 21.

Is this your organization?

Everything on this page comes from Novartis’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.