European Pharmacopoeia, 9th Edition (2016-2019)
         欧州(ヨーロッパ)薬局方 第9版 (EP9.0-9.8)(2016-2019)   
         (Council of Europe)(European Directorate for the Quality of Medicines & Health Care)
         (Main 3-volume plus 8 supplements published during the years
           2016 through 2019)(EP 9.0-9.8
         (書籍版)(USB Stick版)(Online Access版)
            今回より書籍版は本体(Main Volumes)(EP9.0)は3巻セットとなり、本体と約3年間に亘って継続刊行
            The European Pharmacopoeia is a single reference work for the quality of medicines in
            Europe. From January 2017 the 9th Edition will enter into force and replace the 8th Edition
            which is legally binding until 31 December 2016 in the member states of the European
, including the countries of the European Union.
            The texts of the European Pharmacopoeia cover active substances or preperations for
            pharmaceutical use of chemical, animal, human or herbal origin, homoeopathic preparations
            and homoeioathic stocks, antibiotics as well as dosage forms and containers. The texts of
            The European Pharmacopoeia also apply to biologicals, blood and plasma derivatives,
            vaccines and radiopharmaceutical preparations.
            All producers of medicines or substances for pharmaceutical use must apply the quality
            standards of the European Pharmacopoeia for the marketing and use of these
            products in Europe.


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