European Pharmacopoeia, 11th edition; (Main Volume: 11.0 + Supplement 11.1 + Supplement 11.2), Author: EDQM; ISBN: 978-92-871-9105-2, Language: English; Print Format
Product
The subscription consists of 3 issues in English non-cumulative supplements:
- Volume: 11.0 - Publication date: July 2022 - Implementation date: 01 January 2023
- Volume: 11.1 - Publication date: October 2022 - Implementation date: 01 April 2023
- Volume: 11.2 - Publication date: January 2023 - Implementation date: 01 July 2023
Product Details
Author: European Directorate for the Quality of Medicines & HealthCare
Published: EDQM
Publication Date: July 2022
Edition: 11.0 - 11.2
ISBN: 978-92-871-9105-2
Language: English
Dimensions: 30 x 21,6 cm
Approx Weight: 6.270 kg
Product Description
The European Pharmacopoeia 11th Edition book version is non-cumulative.
The 11th 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
Key features:
- New edition, legally binding in 39 European countries as of 1 January 2023 and applied in more than 130 countries worldwide.
-Continuously updated and modernised to meet users' needs.
- Delivers crucial information earlier than any other Pharmacopoeia.
The primary source for quality control standards
The European Pharmacopoeia (Ph. Eur.) is the primary source of official quality standards for medicines and their ingredients in Europe. Ph. Eur. standards provide a scientific basis for the quality control of a product throughout its life cycle, supporting the pharmaceutical industry and healthcare systems.
As laid down in the Council of Europe Convention on the Elaboration of a European Pharmacopoeia and in European Union and national pharmaceutical legislation, these standards are legally binding. They become mandatory on the same date in all states parties to the convention.
The 11th Edition of the Ph. Eur. contains:
- 2,469 monographs (including dosage forms)
- 386 general texts (including general monographs and methods of analysis) and more than 2,800 descriptions of reagents.
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