New legal requirements for submission of product information to poisons centres in EU member states

Author:

de Groot Ronald1,Brekelmans Pieter1,Desel Herbert2,de Vries Irma1

Affiliation:

1. National Poisons Information Center, University Medical Center Utrecht, Utrecht, The Netherlands;

2. Federal Institute for Risk Assessment (BfR), Berlin, Germany

Publisher

Informa UK Limited

Subject

Toxicology,General Medicine

Reference16 articles.

1. Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures, amending and repealing Directives 67/548/EEC and 1999/45/EC, and amending Regulation (EC) No 1907/2006 [Internet]

2. [cited 2017 Mar 29]. Available from: http://eur-lex.europa.eu/legal-content/EN/TXT/?qid=1450695788190&uri=CELEX:02008R1272-20150601

3. de Groot R, Brekelmans PJAM, Meulenbelt J. Article 17 of the Preparations Directive 1999/45/EC is differently implemented in EU member states. RIVM report 233900001/2007 [Internet]

4. [cited 2017 Mar 29]. Available from: http://www.rivm.nl/Bibliotheek/Wetenschappelijk/Rapporten/2007/juli/Article_17_of_the_Preparations_Directive_1999_45_EC_is_differently_implemented_in_EU_Member_States_A_survey_on_how_Poisons_Information_Centres_become_informed_on_dangerous_preparations

5. Harmonisation of Information for Poison Centres. Review according to Article 45(4) of Regulation (EC) No 1272/2008 on classification, labelling and packaging of substances and mixtures. European Commission (Enterprise and Industry) [Internet]. 2012. [cited 2017 Mar 3]. Available from: http://ec.europa.eu/DocsRoom/documents/13223/attachments/1/translations

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