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Siolta Therapeutics

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 673 files tracked
1
legislative file
of 673 tracked
2
with a full position paper
attached to a submission

Counts here are a floor, never a total: they cover the 673 consultation files tracked so far (58,314 submissions, mostly 2021–26), so an organization's real filing history is larger, not smaller.

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Their record over time

Siolta Therapeutics filed 2 positions on 8 Nov 2023, across 1 of the 673 legislative files tracked here, attaching a full position paper 2 times.

What they argued

Medicinal products for human usefiled 8 Nov 2023PDFsource

3 November 2023 PRI response to the public consultation on a PROPOSAL FOR A REGULATION laying down Union procedures for the authorisation and supervision of medicinal products for human use and establishing rules governing the European Medicines Agency, amending Regulation (EC) No 1394/2007 and Regulation (EU) No 536/2014 and repealing Regulation (EC) N 726/2004, Regulation (EC) No 141/2000 and Regulation (EC) No…

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

Medicinal products for human usefiled 8 Nov 2023PDFsource

Confidential | PRI Internal Use Only | Do Not Distribute 3 Novembre 2023 PRI response to the public consultation on a PROPOSAL FOR A DIRECTIVE relating to medicinal products for human use, and repealing Directive 2001/83/EC and Directive 2009/35/EC Deadline: 8 November 2023 – 4000 characters maximum (currently: 3993).

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

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