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2002/0217(COD)

Drug Precursors Regulation

Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL on drug precursors

Stage
In force, reached 18 Feb 2004
In force
In force since 18 Feb 2004 · CELEX 32004R0273
Procedure
Regulation · Ordinary legislative procedure
Last activity
18 Feb 2004
10 acts

Delegated and implementing acts beneath it

By status: 10 published.

ActKindStatusAdoption
Commission Delegated Regulation (EU) 2026/314Delegated · RegulationPublishedQ1 2026
Commission Delegated Regulation (EU) 2025/1475Delegated · RegulationPublishedQ3 2025
Commission Delegated Regulation (EU) 2024/1331Delegated · RegulationPublishedQ1 2024
Commission Delegated Regulation (EU) 2023/196Delegated · RegulationPublishedQ4 2022
Commission Delegated Regulation (EU) 2022/1518Delegated · RegulationPublished12/2021
Commission Delegated Regulation (EU) 2020/1737Delegated · RegulationPublishedQ1 2020
Commission Delegated Regulation (EU) 2018/729Delegated · RegulationPublished10/2017
Commission Delegated Regulation (EU) 2016/1443Delegated · RegulationPublished29/06/2016
Commission Delegated Regulation (EU) 2015/1011Delegated · RegulationPublished24/04/2015
Commission Implementing Regulation (EU) 2015/1013Implementing · RegulationPublished

Titles link to EUR-Lex where the act has been published.

Summary

Generated

Regulation (EC) No 273/2004, in force since 18 August 2005, harmonizes EU controls on drug precursors to prevent diversion. It requires operators and users to obtain licenses (category 1) or registrations (category 2), use customer declarations, document transactions, and notify authorities of suspicious orders. It applies to operators, users, and competent authorities across all Member States.

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Sources: EP Legislative Observatory · EU Law Tracker · EUR-Lex. Record as of 30 Sept 2026. Something wrong on this page? Report an error.

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