Security of supply is a major concern for the Federal Republic of Germany especially with regard to critical medicinal products. Our aim is to reduce dependencies on third countries, strengthen EU production and diversify the supply chains for critical medicinal products. The key industrial challenges for critical medicinal products as outlined in the Call for Evidence document are in line with our local analysis.
Federal Ministry of Health
Public authority · Germany
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.
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Their record over time
Federal Ministry of Health filed 2 positions between 27 Feb 2025 and 28 Aug 2026, across 2 of the 673 legislative files tracked here.
What they argued
DE would like to thank the Commission for the opportunity to give an opinion on the initiative at this early stage. In our view, there is currently no sufficient evidence regarding all of the 148 substances in question to justify their inclusion in Regulations (EC) No. 111/2005 and No. 273/2004, with exception of the following 9 substances: 1.
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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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Everything on this page comes from Federal Ministry of Health’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 If something is wrong or out of date, email info@policyspeak.com and we will correct it.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.
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