The BP is the only comprehensive collection of authoritative official standards for UK pharmaceutical substances and medicinal products
The European Pharmacopeia (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.
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The United States Pharmacopeia and The National Formulary (USP–NF) is a book of public pharmacopeial standards for chemical and biological drug substances, dosage forms, compounded preparations, excipients, medical devices, and dietary supplements.
This English Version of the Japanese Pharmacopoeia, Sixteenth Edition is published to meet the needs of the non-Japanese speaking people. When and if any discrepancy arises between the Japanese original and its English translation, the former is authentic.
The Ayurvedic Pharmacopoeia of India, Part I, Vol IV is legal document of standards for the quality of drugs, substances and preparations included therein (under the Drugs & Cosmetics Act, 1940). The fourth Volume consists of 68 monographs of single drugs of plant origin. Pharmacognosical, chemical and ayurvcdic standards of the parts of the plants
Indian Pharmacopoeia Commission (IPC) is an autonomous institution of the Ministry of Health and Family Welfare which sets standards for all drugs that are manufactured, sold and consumed in India. The set of standards are published under the title Indian Pharmacopoeia (IP)