EP European Pharmacopoeia (Ph. Eur.) 10th Edition: 3 Non-Cumulative Spplements (10.3, 10.4 and 10.5)

Description

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.

Publication and Implementation Dates :

Contents list:

Book/Print Edition:
The 10th Edition consists of 3 initial volumes (10.0) complemented by 8 non-cumulative supplements (10.1 to 10.8). For the convenience of users, direct access to complementary information (Knowledge Database) is included for each monograph and general chapters through a data matrix code. Available in either English or French, the print version contains a subscription key (EPID code) that allows access to online archives.