European Pharmacopoeia Supplement 10.3-10.5
- European Directorate for the Quality of Medicines & HealthCare
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.
Approximately 30% of the content is new or revised compared to Edition 9.0 with 114 new and 683 revised texts.
The Pharmacopoeia you need to comply with in order to market your products in 38 European countries and beyond.
Delivers crucial information earlier than any other Pharmacopoeia.
Contains 2,420 monographs, 374 general texts (including general monographs and methods of analysis) and around 2,780 descriptions of reagents.
The 2020 subscription will consist of the first 3 volumes (10.0) and the first 2 noncumulative updates, 10.1 and 10.2, and will provide access to the Ph. Eur. online archives until 31 December 2020. For the convenience of users, direct access to complementary information (Knowledge Database) is also included for each monograph and general chapters through a data matrix code.
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