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The European Directorate for the Quality of Medicines & HealthCare (EDQM) is a Directorate and partial agreement of the Council of Europe that traces its origins and statutes to the Convention on the Elaboration of a European Pharmacopoeia (an international treaty adopted by the Council of Europe in 1964: ETS 50, [2] Protocol [3]).
EDQM building, Strasbourg, France. While the 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 Commission. The European Pharmacopoeia Commission determines ...
The GEON, which comprises over 70 OMCLs from over 40 different countries, is co-ordinated by the Strasbourg-based European Directorate for the Quality of Medicines & HealthCare (EDQM) of the Council of Europe, an international organisation upholding human rights, democracy and the rule of law in Europe.
Pharmacopoeial reference standards are a subset of pharmaceutical reference standards. They are established for the intended use described in pharmacopeial texts (monographs and general chapters).
Abbrev. [1]Meaning [1] Latin (or Neo-Latin) origin [1]; a.c. before meals: ante cibum a.d., ad, AD right ear auris dextra a.m., am, AM morning: ante meridiem: nocte ...
A subscription-based product of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), MedDRA or Medical Dictionary for Regulatory Activities is a clinically validated international medical terminology dictionary-thesaurus used by regulatory authorities and the biopharmaceutical industry during the regulatory process, from pre-marketing ...
Other major CoE bodies include the European Directorate for the Quality of Medicines & HealthCare (EDQM) [12] and the European Audiovisual Observatory. The headquarters of the Council of Europe, as well as its Court of Human Rights, are situated in Strasbourg, France. The Council uses English and French as its two official languages.
The Falsified Medicines Directive is a legal framework introduced by the European Commission, to improve the protection of public health within the European Union.The directive applies since 2 January 2013.