EU Member States classify drugs and precursors according to the three UN Conventions of 1961, 1971 and 1988 (abbreviated below to UN61, UN71 and UN88), controlling and supervising their legitimate scientific or medical use while taking into account the particular risks to public or individual health.

This Topic Overview looks at the UN system, the EU’s system of pan-European control, and finally gives a table outlining the similarities and differences of the national systems in the EU and Norway.

Please click here to view the classification tables.

Keep up-to-date with drug policy developments by subscribing to the IDPC Monthly Alert.