European Pharmacopoeia 8th Edition 2014 Print (Volume 8.0 ,8.1 and 8.2)

EP2014 The European Pharmacopoeia (Ph. Eur.) defines requirements for the qualitative and quantitative composition of medicines, the tests to be carried out on medicines and on substances and materials used in their production. It covers active substances, excipients and preparations of chemical, animal, human or herbal origin, homoeopathic preparations and homoeopathic stocks, antibiotics, as well as dosage forms and containers. It also includes texts on biologicals, blood and plasma derivatives, vaccines and radiopharmaceutical preparations. The European Pharmacopoeia and its requirements are legally binding in the member states of the European Pharmacopoeia Convention and the European Union. This subscription contains: the base volume 8.0 (published in July 2013 - for implementation January 2014 supplement 8.1 (published in October 2013 - new/revised texts agreed in March 2013 - for implementation in April 2014 supplement 8.2 (published in January 2014 - new/revised texts agreed in June 2013 - for implementation in July 2014 9789287175298 9789287175274 9789287175250