The 9th Edition of the European Pharmacopoeia (EP) main volume and supplements are legally binding and details the qualitative and quantitative composition of medicines, the Tests to be carried out on medicines, on 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.
The EP outlines preparations for pharmaceutical use of chemical, animal, human or herbal origin. It also covers biological, blood and plasma derivatives, vaccines and radiopharmaceutical preparations. The monographs give quality standards for all the main medicines used in Europe.
The 9th Edition consists of all the texts published in the 8th Edition, which may subsequently have been revised or corrected and new texts.
|EP Supplement 9.6
|EP Supplement 9.7
|EP Supplement 9.8
The EP is a subscription product and all orders must be prepaid. Renouf's price includes the shipping costs to deliver the three supplements.