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.
VS
Veeva Systems
Company · United States
not in the EU Transparency RegisterThis organization files on consultations without a register number, so its record here is built from its filings alone. Register facts (staff, costs, accreditations) are not available for it.
2
positions filed
in the 665 files tracked
2
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.
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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 665 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.
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