European Pharmacopoeia — The European Pharmacopoeia of the Council of Europe is a listing of a wide range of active substances and excipients used to prepare pharmaceutical products in Europe. The 2005 edition includes 1800 specific and general monographs, including… … Wikipedia
Certification of suitability of Monographs of the European Pharmacopoeia — Das Certificate of suitability of Monographs of the European Pharmacopoeia (engl., Abk. CEP) ist eine Konformitätsbescheinigung darüber, dass ein Arzneistoff der in einer Monographie des Europäischen Arzneibuches beschriebenen Qualität entspricht … Deutsch Wikipedia
European Directorate for the Quality of Medicines — The European Directorate for the Quality of Medicines of the Council of Europe (EDQM) came into being in its current form in 1996. It consists of the Technical Secretariat of the European Pharmacopoeia Commission long referred to as the European… … Wikipedia
Pharmacopoeia — s issued by private individuals.HistorySome of the earliest pharmacopoeia books were written by Arabian and Persian physicians. [Philip K. Hitti (cf. Dr. Kasem Ajram (1992), Miracle of Islamic Science , Appendix B, Knowledge House Publishers.… … Wikipedia
European Directorate for the Quality of Medicines — Das European Directorate for the Quality of Medicines HealthCare (EDQM), auf französisch Direction européenne de la qualité du médicament (DEQM), auch kurz „Pharmacopée européenne“ genannt, ist die europäische Arzneibuch Kommission und im… … Deutsch Wikipedia
British Pharmacopoeia — Published annually, the British Pharmacopoeia (BP) is a collection of quality standards for UK medicinal substances. It is used by individuals and organizations involved in pharmaceutical research, development, manufacture and… … Wikipedia
Ph. Eur. U. — European Pharmacopoeia unit … Medical dictionary
Ph. Eur. U. — • European Pharmacopoeia unit … Dictionary of medical acronyms & abbreviations
Council of Europe — Not to be confused with European Council or Council of the European Union. Council of Europe Conseil de l Europe … Wikipedia
Medicines and Healthcare products Regulatory Agency — The logo of the MHRA. The Medicines and Healthcare products Regulatory Agency (MHRA) is the UK government agency which is responsible for ensuring that medicines and medical devices work and are acceptably safe. The agency was formed on 1 April… … Wikipedia
Фармакопея — (с др. греч. φαρμακον лекарство, яд и др. греч. ποιη делаю, изготовляю) сборник официальных документов (свод стандартов и положений), устанавливающих нормы качества лекарственного сырья медицинских субстанций,… … Википедия