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Quality standards of the European Pharmacopoeia
Journal of Ethnopharmacology, 2014The European Pharmacopoeia (Ph. Eur.) provides a legal and scientific reference for the quality control of medicines. It is legally binding in the 38 signatory parties of the Convention on the elaboration of a European Pharmacopoeia (37 member states and the European Union).The requirements for a specific herbal drug are prescribed in the corresponding
Anne-Sophie, Bouin, Michael, Wierer
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Medicina nei secoli, 1995
In defining a pharmacopoeia as an instrument for the quality control of medicines in the public health field, the author illustrates the origin, history and development of the European Pharmacopoeia since the Brussels Treaty in 1948. 20 countries are now applying the European Pharmacopoeia standards; they are based on an international Convention, which
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In defining a pharmacopoeia as an instrument for the quality control of medicines in the public health field, the author illustrates the origin, history and development of the European Pharmacopoeia since the Brussels Treaty in 1948. 20 countries are now applying the European Pharmacopoeia standards; they are based on an international Convention, which
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Abstract The roles and principles of operation of the European Directorate for the Quality of Medicines and HealthCare (EDQM), the European Pharmacopoeia (EP) and the British Pharmacopeia (BP) are described.
Phil Ambery +2 more
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Phil Ambery +2 more
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2005
A pharmacopeia is a collection of recommended specifications and other information for therapeutic products, including drug substances (active ingredients), excipients, dosage forms (also called preparations), and other articles. One function of a pharmacopeia is to provide a uniform and public basis onwhich to evaluate these therapeutic products ...
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A pharmacopeia is a collection of recommended specifications and other information for therapeutic products, including drug substances (active ingredients), excipients, dosage forms (also called preparations), and other articles. One function of a pharmacopeia is to provide a uniform and public basis onwhich to evaluate these therapeutic products ...
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Establishment of European pharmacopoeia Mycoplasma reference strains.
Pharmeuropa bio, 2007European Pharmacopoeia (Ph. Eur.) general chapter 2.6.7. Mycoplasma requires for the culture test reference strains of mycoplasma field isolates with fewer than 15 passages for validation and run control and in the test for inhibitory substances. Low passage field isolates of 5 mycoplasma strains (Mycoplasma hyorhinis, Mycoplasma synoviae, Mycoplasma ...
C, Milne, A, Daas
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