Veeva Systems welcomes the opportunity to provide feedback on the targeted revision of EU rules for medical devices and in vitro diagnostics. Our response highlights the urgent need for a mandatory, structured electronic submission format to strengthen Europes data governance, enhance efficiency, and accelerate patient access to safe, innovative technologies.
Veeva Systems
Company · United States
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.
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Their record over time
Veeva Systems filed 2 positions between 10 Sept 2025 and 6 Oct 2025, across 2 of the 326 legislative files tracked here, attaching a full position paper 2 times.
What they argued
Veeva Systems welcomes the opportunity to provide feedback on the proposed European Research Area (ERA) Act. Our attached response highlights challenges and recommendations to strengthen Europes research capacity, streamline multi-country study execution, and improve patient access.
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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.
- Wirtschaftskammer Österreich · 2 files in common
- Deutsche Industrie- und Handelskammer · 2 files in common
- HOPE (EUROPEAN HOSPITAL AND HEALTHCARE FEDERATION) · 2 files in common
- BioMed Alliance · 2 files in common
- University of Groningen · 2 files in common
Showing 5 of 7.
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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.