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European Pharmacopoeia, 10th Edition 欧州薬局方 (本体10.0-補遺10.2) 書籍版

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European Pharmacopoeia, 10th Edition 欧州薬局方 (本体10.0-補遺10.2) 書籍版





European Pharmacopoeia 10th Edition (10.0-10.2)
欧州薬局方 第10版 (本体10.0-補遺10.2)
発行元 EDQM
発行年/月 10.0 (2019年7月) 10.1 (2019年10月) 10.2 (2020年1月)
装丁 ハードカバー
ご請求方法について 本体10.0の納品時にご請求とさせて頂きます
発送予定 在庫有り 1-2営業日以内に発送致します


◆Why do you need the European Pharmacopoeia?

The European Pharmacopoeia (Ph. Eur.) is a single reference work for the quality control of medicines. The official standards published within provide a scientific basis for quality control during the entire life cycle of a product.

These standards are legally binding - as laid down in the Council of Europe’s Convention on the elaboration of a European Pharmacopoeia and in EU and national pharmaceutical legislation. Ph. Eur. quality standards become mandatory on the same date in all signatory member states of the Convention.

◆The 10th Edition at a glance

- The Pharmacopoeia you need to comply with in order to market your products in 38 European countries and beyond.
- It delivers crucial information earlier than any other pharmacopoeia.
- With 114 new and 683 revised texts, approximately 30% of the content is new or revised compared to Edition 9.0.
- It contains 2 420 monographs, 374 general texts (including general monographs and methods of analysis) and around 2 780 descriptions of reagents.