European Pharmacopoeia 9th edition - English Print
- European Pharmacopoeia Commission, Council of Europe European Directorate for the Quality of Medicines (EDQM)
The 9th Edition of the European Pharmacopoeia (EP), main volume and supplements, is legally binding and details the qualitative and quantitative composition of medicines, the tests to be carried out on medicines, the raw materials used in the production of medicines and on the intermediates of synthesis.
The EP is a single reference work for the quality control of medicines in Europe. 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.
Applicable in 37 European countries and used in over 100 worldwide
Delivers crucial information earlier than any other Pharmacopoeia
Over 50% new or revised texts compared to the 8th Edition
Includes free access to the online archive, access to the 9th Edition available only from 01/01/17
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