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Takeda Pharmaceuticals International AG

Company · Japan · EU Transparency Register 815176718826-78

8
positions filed
in the 665 files tracked
5
legislative files
of 665 tracked
2
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 1210 companies & groups on this site, they rank #278 by legislative files engaged, a count of participation, not a measure of influence.

1.8
declared lobbying FTE
self-declared
€1M+
declared costs / yr (floor)
3
EP accreditations
as declared to the register
2015
in the register since

Declares membership of

  • Takeda is a member of European Federation of Pharmaceutical Industries and Associations (EFPIA) and Vaccines Europe.
  • Takeda is member of EUCOPE (European Confederation of Pharmaceutical Enterpreneurs).
  • Takeda is also member of PPTA Europe, Japanese Business Council in Europe and MedTech Europe.

Self-declared to the EU Transparency Register (snapshot 14 Oct 2026).

Register category
Companies & groups
Head office
Zurich, Switzerland
EU office
Brussels

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.

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Their record over time

Takeda Pharmaceuticals International AG filed 8 positions between 14 Dec 2020 and 8 Oct 2026, across 5 of the 665 legislative files tracked here, attaching a full position paper 2 times.

2020 · 1 filed2021 · 2 filed2022 · 1 filed2023 · 2 filed2026 · 2 filed

What they argued

Medicinal products for human usefiled 24 Oct 2023PDFsource

Takeda is a patient-focused, values-based, R&D-driven biopharmaceutical company committed to delivering highly innovative medicines and transformative care to improve lives worldwide. Takeda supports the Commissions objectives for the revision of the EU pharmaceutical legislation: the ambition for timely access and enhanced availability of medicines across Member States, more efficient regulatory processes, and an…

Medicinal products for human usefiled 24 Oct 2023PDFsource

Takeda is a patient-focused, values-based, R&D-driven biopharmaceutical company committed to delivering highly innovative medicines and transformative care to improve lives worldwide. Takeda supports the Commissions objectives for the revision of the EU pharmaceutical legislation: the ambition for timely access and enhanced availability of medicines across Member States, more efficient regulatory processes, and an…

Medicinal products for human usefiled 27 Apr 2021source

Takeda is a patient-focused, values-based, R&D-driven biopharmaceutical company committed to delivering highly innovative medicines and transformative care to improve lives worldwide. The Covid-19 crisis has shown that Europe needs to reflect on how to deliver resilient health systems whilst remaining a competitive actor on the global stage.

European Biotech Actfiled 4 Aug 2026source

Takeda welcomes the European Commissions proposal for a European Biotech Act and supports its overall ambition to strengthen Europes biotechnology and life sciences ecosystem. The Biotech Act is a positive and necessary step to reinforce Europes position in innovative biotechnologybased medicines.

Standards of quality and safety for substances of human origin intended for human applicationfiled 8 Sept 2022source

As a patient-focused, values-based, R&D-driven global biopharmaceutical company, Takeda welcomes the proposal for a new Regulation on Substances of Human Origin (SoHO) and the Commission's efforts to help ensure legislation can respond to new scientific and technical developments while meeting the needs of European patients and safeguarding donor health and safety.

Standards of quality and safety for substances of human origin intended for human applicationfiled 14 Dec 2020source

Takeda is a global, patient-focused, values-based and R&D-driven biopharmaceutical company committed to better health and a brighter future. We welcome the initiative to review EU legislation on Blood, Tissues and Cells (BTC) to ensure it considers new scientific and technical developments and includes the necessary provisions to meet donor and patient needs, while ensuring their safety.

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

Takeda is a global, patient-focused, values-based and R&D-driven biopharmaceutical company committed to bringing better health to people and a brighter future to the world. Takeda believes this review should focus on supporting the sustainable development of innovative therapies addressing unmet medical needs and access pathways for patients to benefit for these therapies in a timely and equitable manner.

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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 107.

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Everything on this page comes from Takeda Pharmaceuticals International AG’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.