European Pharmacopoeia 10th edition 10.3-10.5
- European Directorate for the Quality of Medicines & HealthCare
The 10th 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 39 European countries and used in over 120 worldwide.
Delivers crucial information earlier than any other Pharmacopoeia.
Provides new and revised text.
Available in print and electronic versions, with direct access to complementary information (EDQM Knowledge Database).
|Format||Electronic||Published||15 May 2020|
|Availability||Out of stock - available to order||Delivery||Delivery options and charges|