Third party beneficiary status occurs when data is available

EUR-Lex Access to European Union law

Commission Delegated Regulation (EU) 2016/161 of 2 October 2015 supplementing Directive 2001/83 / EC of the European Parliament and of the Council by laying down detailed rules for the safety features appearing on the packaging of medicinal products for human use (Text with EEA relevance)

Commission Delegated Regulation (EU) 2016/161 of October 2, 2015 supplementing Directive 2001/83 / EC of the European Parliament and of the Council by laying down precise provisions on the safety features on the packaging of medicinal products for human use (text with EEA relevance )

Commission Delegated Regulation (EU) 2016/161 of October 2, 2015 supplementing Directive 2001/83 / EC of the European Parliament and of the Council by laying down precise provisions on the safety features on the packaging of medicinal products for human use (text with EEA relevance )

OJ L 32, 9.2.2016, p. 1–27 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

In force: This act has been changed. Current consolidated version: 01/01/2021

ELI: http://data.europa.eu/eli/reg_del/2016/161/oj