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  2. European Pharmacopoeia - Wikipedia

    en.wikipedia.org/wiki/European_Pharmacopoeia

    The quality standards of the European Pharmacopoeia apply throughout the entire life-cycle of a product, and become legally binding and mandatory on the same date in all thirty-nine (39) signatory states, which include all European Union member states. Several legal texts make the European Pharmacopoeia mandatory in Europe. [1]

  3. European Directorate for the Quality of Medicines & HealthCare

    en.wikipedia.org/wiki/European_Directorate_for...

    The European Pharmacopoeia: setting quality standards for Europe and beyond and supplying pharmaceutical reference standards [ edit ] Published and regularly updated by the EDQM/ Council of Europe in English and French, the two official languages of the Council of Europe, the Ph. Eur. is a compendium of official quality standards for medicines ...

  4. Drug reference standard - Wikipedia

    en.wikipedia.org/wiki/Drug_reference_standard

    Pharmacopeial reference standards are available from various pharmacopoeias such as United States Pharmacopeia and the European Pharmacopoeia. Where pharmacopoeial tests or assays call for the use of a pharmacopoeial reference standard, only those results obtained using the specified pharmacopoeial reference standard are conclusive. [citation ...

  5. EudraLex - Wikipedia

    en.wikipedia.org/wiki/EudraLex

    Eudralex,The Rules Governing Medicinal Products in the European Union, European Communities Commission. Directorate-General for Industry, Pharmaceuticals and Cosmetics. Vol. 1: Pharmaceutical legislation: medicinal products for human use.

  6. Category:Pharmacopoeias - Wikipedia

    en.wikipedia.org/wiki/Category:Pharmacopoeias

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  7. International Council for Harmonisation of Technical ...

    en.wikipedia.org/wiki/International_Council_for...

    In the 1980s, the European Union began harmonising regulatory requirements. In 1989, Europe, Japan, and the United States began creating plans for harmonisation. The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) was created in April 1990 at a meeting in Brussels.

  8. British Pharmacopoeia - Wikipedia

    en.wikipedia.org/wiki/British_Pharmacopoeia

    The British Pharmacopoeia (BP) is the national pharmacopoeia of the United Kingdom.It is an annually published collection of quality standards for medicinal substances in the UK, which is used by individuals and organisations involved in pharmaceutical research, development, manufacture and testing.

  9. List of abbreviations used in medical prescriptions - Wikipedia

    en.wikipedia.org/wiki/List_of_abbreviations_used...

    Pharmacopoeia Britannica: British Pharmacopoeia Ph.Eur. Pharmacopoeia Europaea: European Pharmacopoeia Ph.Int. Pharmacopoeia Internationalis: International Pharmacopoeia pig./pigm. pigmentum: paint p.m. post meridiem: evening or afternoon p.o. per os: by mouth or orally AMA style avoids use of this abbreviation (spell out "orally") ppt ...