Supplementary protection certificate for medicinal products. Recast
This dossier is a recast of the rules on supplementary protection certificates for medicinal products. The amendments address protection conditions tied to a basic patent, avoiding overprotection through one certificate per product, the maximum duration of protection and paediatric extension, a centralised application examined under an Office with national examiners, fees, third-party observations, Boards of Appeal, generics and biosimilars, and disclosure of public financial support for research.
Procedure timeline
- Committee amendments tabled14 Nov 2023
- Plenary vote — Adopted28 Feb 2024 · On the Commission proposal (the draft law)
- In progress — not yet concluded
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 →
- 28 Feb 2024Main voteAdoptedOn the Commission proposal (the draft law)Official label: Proposition de la Commission · what was voted ↗526 for23 against70 abstentions86 did not voteForAgainstAbst.
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Vote data: HowTheyVote.eu (ODbL, attribution) / European Parliament · roll-call votes only
How groups usually vote on similar files
Based on 56 past main roll-call votes on JURI-responsible procedures, Jul 2019 → 2026-07-04.
Statistical baseline from past roll-call votes; not a forecast. · roll-call votes only
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Official amendment documents
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Explore the graphMembers who amended this procedure
3 Members · by amendment countThe amendments, in full text
216 amendmentsEvery amendment as tabled — original text, proposed change and justification, with a link to the official PDF.