Specific rules relating to medicinal products for human use intended to be placed on the market of Northern Ireland
A legislative proposal on specific rules for medicinal products for human use intended for the market of Northern Ireland. Amendments address the prohibition on displaying certain safety features, except anti-tampering device measures, on the packaging of those products, their removal or covering, the role of the qualified person and record-keeping, authorisation of new and innovative products by United Kingdom competent authorities, and the conditions and written guarantees required.
Procedure timeline
- Committee amendments tabled12 Apr 2023
- Plenary vote — Passed9 May 2023 · On the Commission proposal (the draft law)
- Procedure completed
Plenary votes
1 roll-call votesIn plenary, Parliament usually votes in steps: first on amendments to the text (sometimes split into parts, so Members can accept one half of a sentence and reject the other), then on the text as a whole. The “main vote” is the one that adopts or rejects the text itself. Each vote below shows exactly which step it was. How voting works →
- 9 May 2023Main votePassedoutcome from totalsOn the Commission proposal (the draft law)Official label: Proposition de la Commission · what was voted ↗617 for3 against6 abstentions79 did not voteForAgainstAbst.
Click a group to see each Member’s position.
Vote data: HowTheyVote.eu (ODbL, attribution) / European Parliament · roll-call votes only
Official amendment documents
Connections
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Explore the graphMembers who amended this procedure
2 Members · by amendment countThe amendments, in full text
9 amendmentsEvery amendment as tabled — original text, proposed change and justification, with a link to the official PDF.