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General eu classification guidelines for preparations a through g: >> http://soa.cloudz.pw/download?file=general+eu+classification+guidelines+for+preparations+a+through+g << (Download)
General eu classification guidelines for preparations a through g: >> http://soa.cloudz.pw/read?file=general+eu+classification+guidelines+for+preparations+a+through+g << (Read Online)
Oct 3, 2003 ENTERPRISE DIRECTORATE-GENERAL Commission Regulation (EC) No 1084/2003 concerning the examination of variations to . mass (250mg/g) or per unit of volume (2mg/ml) or in percentage (5%). For the purpose of this Guideline: - for single-dose preparations, total use, the strength is defined as
The European. Chemicals Agency does not accept any liability with regard to the use that may be made of the information contained in this document. Version General overview. 2.1 Legal background. CLP is the EU Regulation on classification, labelling and packaging of substances and mixtures. It is based on the
in pharmacies only following initial medical diagnosis or available on general sale, as the case may be. Purpose. This guideline is for use by marketing authorisation holders applying to change the classification for supply of a . reflected in the label (as provided for in Article 54 g) and n) of Directive 2001/83/EC and/or.
Classification and labelling identify hazardous chemicals and inform users about their hazards through standard symbols and phrases. They need to be harmonised to ensure good CLP sets general packaging standards to ensure the safe supply of hazardous substances and mixtures. In the case of certain hazards,
GUIDANCE DOCUMENT ON EC REGULATION ON FLAVOURINGS. General introduction. 5. Chapter Ia (Articles 1 and 2) – Subject Matter and Scope. 7. 1. Flavour precursor (Article 3.2 (g)). 12. 8. .. Substances and (Natural) Flavouring Preparations in the EU" (See Attachment II to this Guidance Document) to bring.
Mar 18, 2011 THE RULES GOVERNING MEDICINAL PRODUCTS IN THE EUROPEAN UNION. VOLUME 10 - GUIDANCE 1 For the purposes of this document, references to the EU, EU Member States or Member States should As a general rule, the documentation requirements in the application dossier for IMPs. 7.
GUIDANCE. Guidance on the Application of the CLP. Criteria. Guidance to Regulation (EC) No 1272/2008 on classification, labelling and packaging (CLP) of with regard to the use that may be made of the information contained in this document. Guidance on the Application of CLP Criteria. Reference: ECHA-17-G-21-EN.
The variations regulation lays down general rules on the types and classification of variations in Articles 2 and 3 Definitions relevant to this guideline are provided in Directive 2001/82/EC, Directive. 2001/83/EC . Products, and with the guideline on declaration of herbal substances and herbal preparations in. (traditional)
The present MEDDEV is part of a set of guidelines relating to questions of application of EU Directives on medical devices. They are not legally CONTENTS. Pages. 1. PURPOSE AND PHILOSOPHY OF MEDICAL DEVICE. CLASSIFICATION. 2. PRACTICAL RELEVANCE OF CLASSIFICATION. 2.1. General requirements.
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