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The European Pharmacopoeia[1] ( Pharmacopoeia
Pharmacopoeia
Europaea, Ph. Eur.) is a major regional pharmacopoeia which provides common quality standards throughout the pharmaceutical industry in Europe
Europe
to control the quality of medicines, and the substances used to manufacture them.[1] It is a published collection of monographs which describe both the individual and general quality standards for ingredients, dosage forms, and methods of analysis for medicines.[1] These standards apply to medicines for both human and veterinary use.[1]

Contents

1 Legal
Legal
basis 2 The European Pharmacopoeia
Pharmacopoeia
Commission 3 Publication 4 References 5 External links

Legal
Legal
basis[edit] The European Pharmacopoeia
Pharmacopoeia
has a legally binding character. It is used as an official reference to serve public health,[1] and is part of the regulatory requirements for obtaining a Marketing Authorisation Application (MAA) for a medicinal (human or veterinary) product.[1] Pharmacopoeia
Pharmacopoeia
Europaea quality standards apply throughout the entire life-cycle of a product, and become legally binding and mandatory on the same date in all thirty-eight (38)[2] signatory states and the European Union
European Union
member states. Several legal texts make the European Pharmacopoeia
Pharmacopoeia
mandatory in Europe.[1] The Convention on the Elaboration of a European Pharmacopoeia
Pharmacopoeia
(CETS 50)[3] which was adopted by the Council of Europe in 1964, laid the groundwork for the development of the European Pharmacopoeia. In 1994, a Protocol (ETS No. 134)[1][4] was adopted, amending the Convention to prepare for the accession of the European Union (EU), and defining the respective powers of the European Union and its Member States within the European Pharmacopoeia
Pharmacopoeia
Commission. European Union
European Union
Directive 2001/82/EC[5] and Directive 2001/83/EC,[6] (as amended) state the legally binding character of European Pharmacopoeia
Pharmacopoeia
texts for Marketing Authorisation Applications (MAA). All manufacturers of medicines or substances for pharmaceutical use therefore must apply the European Pharmacopoeia
Pharmacopoeia
quality standards in order to be able to market and use these products in Europe.[1] As of November 2016, thirty-seven (37) member states and the European Union are signatories to the Convention on the Elaboration of a European Pharmacopoeia. Twenty-six (26) countries from all continents are part of its observers, as is the World Health Organization
World Health Organization
(WHO) and the Taiwan Food and Drug Administration (TFDA). The European Pharmacopoeia
Pharmacopoeia
Commission[edit]

EDQM building, Strasbourg, France

While the European Directorate for the Quality of Medicines
European Directorate for the Quality of Medicines
& HealthCare (EDQM), a directorate of the Council of Europe, provides scientific and administrative support for the European Pharmacopoeia, the governing body is the European Pharmacopoeia
Pharmacopoeia
Commission. The European Pharmacopoeia
Pharmacopoeia
Commission determines the general principles applicable to the elaboration of the European Pharmacopoeia. It also decides the work programme, sets up and appoints experts to the specialised groups responsible for preparing monographs, adopts these monographs, and recommends time limits for the implementation of its decisions within the territories of the contracting parties. This Commission meets in Strasbourg, France, three times a year, to adopt texts proposed by its groups of experts, and to decide on its programme of work and general policies. Items are added to the work programme in response to requests received by the European Directorate for the Quality of Medicines & HealthCare from the Member States and their national authorities, based on current scientific and health issues in Europe. Each national delegation has one vote. In all technical questions, the decisions of the Commission are taken by a unanimous vote of the national delegations that cast a vote. Member States' representatives are from health authorities, national pharmacopoeia authorities, universities or industry; and are appointed by the national authorities on the basis of their expertise. Representatives of the twenty-eight (28) observers are invited to attend the sessions, but cannot vote. The current Chair of the Commission is Dr Tobias Gosdschan, who was elected in March 2016.[2] Dr Gosdschan term for Chair is three years, and runs in parallel with other members of the Commission's Presidium.[2] Publication[edit] The 1st Edition of the European Pharmacopoeia
Pharmacopoeia
was published in 1969, and comprised 120 texts. The 9th Edition,[7] was published in July 2016 and is currently in force. It contains some 2,300 monographs, and more than 350 general chapters, illustrated with diagrams or chromatograms, and over 2,500 descriptions of reagents. With 121 new and 1,403 revised texts, over 50 percent of the 9th Edition's content is new compared to the 8th Edition. It consists of three initial volumes (9.0), and will culminate in a collection of eight non-cumulative supplements (9.1 to 9.8).[7] A new edition is published every three years: in both English and French,[7] by the Council of Europe. It is made available in print and electronic (online and downloadable) versions; the online version is also accessible from smartphones and tablet computers.[7] Translations into other languages are published by the Member States themselves. For example, a German version is jointly published by Austria, Germany and Switzerland. References[edit]

Europe
Europe
portal Medicine
Medicine
portal Pharmacy and pharmacology portal

^ a b c d e f g h i "European Pharmacopoeia
Pharmacopoeia
(Ph. Eur.) – Background & Mission". www.EDQM.eu. European Directorate for the Quality of Medicines & HealthCare (EDQM). Retrieved 8 November 2016.  ^ a b c "155th Session of the European Pharmacopoeia
Pharmacopoeia
Commission (21-22 June 2016)" (pdf). www.EDQM.eu (Press release). Strasbourg, France: European Directorate for the Quality of Medicines
European Directorate for the Quality of Medicines
& HealthCare (EDQM). 30 June 2016. Retrieved 8 November 2016.  ^ "Details of Treaty No.050, Convention on the Elaboration of a European Pharmacopoeia". www.CoE.int. Treaty Office, Council of Europe. Retrieved 8 November 2016.  ^ "Details of Treaty No.134, Protocol to the Convention on the Elaboration of a European Pharmacopoeia". www.CoE.int. Treaty Office, Council of Europe. Retrieved 8 November 2016.  ^ "Directive 2001/82/EC of the European Parliament and of The Council of 6 November 2001 on the Community code relating to veterinary medicinal products" (pdf). ec.Europa.eu - Official Journal of the European Communities. European Union. 6 November 2001. Retrieved 8 November 2016.  ^ " Directive 2001/83/EC of the European Parliament and of The Council of 6 November 2001 on the Community code relating to medicinal products for human use" (pdf). Eur-Lex.Europa.eu - Official Journal of the European Communities. European Union. 6 November 2001. Retrieved 8 November 2016.  ^ a b c d "European Pharmacopoeia
Pharmacopoeia
(Ph. Eur.) 9th Edition". www.EDQM.eu. European Directorate for the Quality of Medicines
European Directorate for the Quality of Medicines
& HealthCare (EDQM). Retrieved 8 November 2016. 

External links[edit]

Wikimedia Commons has media related to European Pharmacopoeia.

European Directorate for the Quality of Medicines
European Directorate for the Quality of Medicines
& HealthCare (EDQM Council of Europe) — official website

European Pharmacopeia 9th Edition EDQM store

Council of Europe European Commission — the executive of the European Union
European Union
(EU) European Medicines Agency (EMA) EUR-Lex –

.