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hollandbio

Industry association · Netherlands · EU Transparency Register 776438619820-95

15
positions filed
in the 665 files tracked
11
legislative files
of 665 tracked
13
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 #300 by legislative files engaged, a count of participation, not a measure of influence.

0.2
declared lobbying FTE
self-declared
€25K+
declared costs / yr (floor)
0
EP accreditations
as declared to the register
2015
in the register since

Declares membership of

  • EuropaBio: https://www.europabio.org/
  • ICBA: https://internationalbiotech.org/

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

Register category
Trade and business associations
Registered as
Hollandbio
Head office
The Hague, Netherlands

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

hollandbio filed 15 positions between 6 Jan 2021 and 28 Sept 2026, across 11 of the 665 legislative files tracked here, attaching a full position paper 13 times.

2021 · 2 filed2023 · 2 filed2025 · 6 filed2026 · 5 filed

What they argued

Circular Economy Actfiled 5 Nov 2025PDFsource

A circular economy is indispensable for a future world. By using materials smarter, reducing waste and making the most of raw materials, we are building a society that is not only climate-friendly, but also economically strong and competitive. The urgency to make this transition is widely recognised, but the role of biotech in accelerating it remains underscored.

Filed in Dutch · English published by the European Commission

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 30 Jul 2026PDFsource

IVDR/MDR revision: cautiously clarify a viable route from lab to practice When you are ill, you just want one thing: improve. Prefer to stay healthy. At a time when bespoke health is emerging thanks to advances in diagnostics, disease models and treatment options, hollandbio sees innovative diagnostics that help make bespoke work possible in practice as stumbling away from a forest of rules and procedures, including…

Filed in Dutch · English published by the European Commission

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

Diagnostics as a key to bespoke health When you are ill, you want only one thing: improve. Prefer to stay healthy. The right treatment at the right time for the right patient is getting closer, thanks to advances in diagnostics and treatments. Only these innovations need to achieve this in practice. At a time when the technology is ready to deliver bespoke health, it is stuck in a forest of rules and procedures.

Filed in Dutch · English published by the European Commission

28th regime corporate legal framework – EU Inc.filed 25 Sept 2025PDFsource

1 Consultation input — The Hague, 11 August 2025 Transform the EU from company nursery to powerhouse Europe is known as a forward-thinking continent, where knowledge and innovation have been at its core for centuries. What was true then remains relevant today. Yet, we are at risk of being overtaken by countries like the United States and China. That’s unfortunate - and not without consequences.

Opening of the attached position paper · the full paper is on the Commission’s record (source link above)

Medicinal products for human usefiled 17 Jul 2023PDFsource

Hollandbio’s response to the main lines of the review of the EU’s general pharmaceutical legislation can be found on our website: https://www.hollandbio.nl/nieuws/grijp-die-kans-geneesmiddelen-sneller-beter-slimmer-goedkoper-en-groener-beschikbaar-dankzij-herziening-eu-geneesmiddelenwetgeving/ in addition to this, in the excel attached, we set out our more detailed position with regard to the different measures.

Filed in Dutch · English published by the European Commission

Medicinal products for human usefiled 26 Apr 2021source

HollandBIO, the Dutch biotech industry association, appreciates the opportunity to provide feedback on the roadmap towards the evaluation and revision of the general pharmaceutical legislation to further improve and accelerate patients’ access to safe and affordable medicines and to support innovation in the EU pharmaceutical industry. An ambition very close to our heart.

European Biotech Actfiled 5 Aug 2026PDFsource

Hollandbio, the Dutch biotech association, welcomes the ambition to strengthen biotech as one of Europes key technologies for health, sustainability, resilience and economic prosperity. More than ever, global challenges and geopolitics underline biotechs strategic importance.

European Biotech Actfiled 10 Jun 2025PDFsource

Europe worked hard to become a leader in biotech. But while the rest of the world is taking the next step, we are blocking ourselves. Innovations get stuck in outdated rules and fragmented regulations, talent moves elsewhere, and other continents capitalize on European breakthroughs.

Biotech Act IIfiled 10 Jun 2026PDFsource

Biotechnology and biomanufacturing are critical for Europes future competitiveness, sustainability and strategic autonomy. While the EU has a strong scientific base and broad political support for biotechnology, its potential remains underutilised due to persistent structural barriers that limit scale-up, market entry and uptake.

Plants obtained by certain new genomic techniques and their food and feedfiled 3 Nov 2023PDFsource

At hollandbio, the Dutch biotech association, we are convinced that biotech makes life better. To capitalize on the opportunities of the global biorevolution for health, sustainability, and the economy, a paradigm shift is needed. Instead of amending the current outdated laws and regulations for genetic modification, hollandbio prefers a fresh start with a clean slate.

Plants obtained by new genomic techniques: information requirements and verification of category 1 statusfiled 28 Sept 2026source

Hollandbio is the Dutch industry association for biotechnology companies, representing start-ups, scale-ups, established companies and multinational enterprises. Our members include plant breeders and other companies that develop and apply new genomic techniques. Drawing on their scientific expertise and practical experience, we welcome the opportunity to provide input implementing act for Category 2 NGT plants.

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

HollandBIO, the Dutch biotech industry association, appreciates the opportunity to provide feedback on the inception impact assessment on the revision of the EU legislation on medicines for children and rare diseases. We endorse the four objectives for the revision of the two Regulations. We acknowledge there is room to improve and strengthen the effectiveness of the legislation.

Revision of the Rescue and Restructuring Guidelinesfiled 14 Nov 2025PDFsource

Europe has always been a continent of pioneersturning challenges into opportunities and building a future on knowledge, courage, and collaboration. Our leadership in innovation is no coincidence; its the result of decades of smart investment and bold choices.

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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 464.

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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.