Analysis of PVC plasticizers in medical devices and infused solutions by GC–MS

Author:

Bourdeaux Daniel,Yessaad Mouloud,Chennell Philip,Larbre Virginie,Eljezi Teuta,Bernard Lise,Sautou Valerie

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry

Reference23 articles.

1. European Union, Regulation (EC) No. 1272/2008 of the European Parliament and of the Council 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, 2008.

2. European Union, DIRECTIVE 2007/47/EC OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 5 September 2007 amending Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, Council Directive 93/42/EEC concerning medical devices and Directive 98/8/EC concerning the placing of biocidal products on the market.

3. French law n° 2012–1442 of december 24, 2012 to the suspension of the manufacture, import, export and placing on the market of any specializing in food packaging containing bisphenol A (1) journal officiel de la république française n°0300, 26 décembre 2012 page 20395.

4. Amendment n°1610 to the French law n° 2012–1442 of 24 décembre 2012, voted 10 April, 10 2015.

5. Scientific Committee on Emerging and Newly-Identified Health Risks, opinion on the safety of medical devices containing dehp- plasticized pvc or other plasticizers on neonates and other groups possibly at risk, accessed .

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