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    British Pharma

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    Saurabh Deoli
    The British Pharmacopoeia (BP) is an annual publication that establishes quality standards for pharmaceutical substances used in the UK. It is used by those involved in drug research, development, manufacturing, and testing. The BP was first published in 1864 and has the legal basis to set standards as recommended by the Commission on Human Medicines and notified to the European Commission. The document outlines the history and purpose of the BP in establishing authoritative quality standards for medications in use in the UK.

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    British Pharma

    Uploaded by

    Saurabh Deoli
    232 views12 pages
    The British Pharmacopoeia (BP) is an annual publication that establishes quality standards for pharmaceutical substances used in the UK. It is used by those involved in drug research, development, manufacturing, and testing. The BP was first published in 1864 and has the legal basis to set standards as recommended by the Commission on Human Medicines and notified to the European Commission. The document outlines the history and purpose of the BP in establishing authoritative quality standards for medications in use in the UK.

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    British Pharmacopia

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    The British Pharmacopoeia (BP) is an annual publication that establishes quality standards for pharmaceutical substances used in the UK. It is used by those involved in drug research, development, manufacturing, and testing. The BP was first published in 1864 and has the legal basis to set standards as recommended by the Commission on Human Medicines and notified to the European Commission. The document outlines the history and purpose of the BP in establishing authoritative quality standards for medications in use in the UK.

    Copyright:

    Attribution Non-Commercial (BY-NC)
    Download as PPTX, PDF, TXT or read online from Scribd
    Download as pptx, pdf, or txt
    232 views12 pages

    British Pharma

    Uploaded by

    Saurabh Deoli
    The British Pharmacopoeia (BP) is an annual publication that establishes quality standards for pharmaceutical substances used in the UK. It is used by those involved in drug research, development, manufacturing, and testing. The BP was first published in 1864 and has the legal basis to set standards as recommended by the Commission on Human Medicines and notified to the European Commission. The document outlines the history and purpose of the BP in establishing authoritative quality standards for medications in use in the UK.

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    Download as PPTX, PDF, TXT or read online from Scribd
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    The key takeaways are that the British Pharmacopoeia (BP) is an annual publication that sets quality standards for UK medical substances. It is used by those involved in pharmaceutical research, development, manufacture and testing.

    The legal basis for the BP is that it is published for the UK Health Ministers on the recommendation of the Commission on Human Medicines in accordance with the Medicines Act 1968. It is also notified in draft to the European Commission in accordance with Directive 99/34/EEC.

    The regulation of medicinal products by officials in the UK dates back to the reign of King Henry VIII from 1491-1547. The first list of approved drugs was the London Pharmacopoeia published in 1618. The first edition of the British Pharmacopoeia was published in 1864 and was one of the first attempts to harmonize pharmaceutical standards.

    By - Saaurabh Deoli IBT 4th sem Apeejay Stya University

    The BP is an annual published collection of quality standards for UK medical substances . It is used by individuals and organizations involved in pharmaceutical research , development , manufacture and testing .

    Introduction

    BP is published for the Health Ministers of the United Kingdom on the recommendation of the Comisson on Human Medicines in accordance with section 99(6) on the Medicines Act 1968 .
    It is notified in draft to the European Comisson in accordance with Directive 99/34/EEC

    Legal Basis

    The regulation of medicinal products by officials in the United Kingdom dates back to reign of King Henry Vlll (1491-1547) . The first list of approved drugs with information on how they should be prepared was the London Pharmacopoeia published in 1618. The first edition of the British Pharmacopoeia was published in 1864 and was one of the first attempts to harmonize pharmaceutical standards

    History

    The BP contributes significally to the overall Control of the quality of medicinal products by providing an authoritive statement of the quality that a product , material is expected at the period of use . The Comission on Human Medicines wishes to record its appreciation of the services of all those who have contributed to this important work .

    Mission and Preface

    The first British Pharmacopoeia was published in the English language in 1864. The latest edition (2013) of British pharmacoepia is avilable in market .

    Publications

    To promote the highest standards for the drugs for use in humans and animals within practical limits of the technologies available for manufacturing and analysis

    Vision

    To bing new editions and supplements of the British Pharmacopoeia at regular intervals . To accelerate the process of preperation , certification and distribution of IP Reference Substances . To establish working relations with other Pharmacopoeial Agencies .

    Mandate

    World is becoming closer and cooperation is the way of sucess

    http://en.wikipedia.org/wiki/British_Phar macopoeia http://www.who.int/medicines/areas/quali ty_safety/quality_assurance/resources/Bri tish_Pharmacopoeia.pdf http://www.authorstream.com/Presentati on/netguru-80198-pharmacopoeia-ippharmacy-usp-bp-science-technology-pptpowerpoint/

    References

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