PHARMACOPOEIA

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All about PHARMACOPOEIA

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Presentation Transcript

PHARMACOPOEIA : 

PHARMACOPOEIA WHAT IS Pharmacopoeia is a book or encyclopedia of Drugs Standards, their formulas, Methods for making medicinal preparations and other related information's which is published under the jurisdiction of government body.

WHY : 

WHY To Control the Quality of Medicine as per standard . To Ensure the public health. To Support the availability of safe, effective, good-quality pharmaceutical care for all.

USP/NFThe Standard Of Quality : 

USP/NFThe Standard Of Quality ONE SOURCE MANY ANSWARS This Unique Book of US Pharmacopoeia Is Made Especially For ARABSWELL

USP/NFMission and Preface : 

USP/NFMission and Preface The United States Pharmacopoeia promotes the public health and benefits practitioners and patients by disseminating authoritative standards and information developed by its volunteers for medicines, other health care technologies, and related practices used to maintain and improve health and promote optimal health care delivery Working with many constituencies and stakeholders around the world, USP's compendial activities support the availability of safe, effective, good-quality pharmaceutical care for all.

USP/NFHISTORY : 

USP/NFHISTORY First edition  December 15, 1820. Second edition  1830. Next each edition at 10-year intervals up to 1842. Next each edition at 05-year intervals from 1942 to 2000 After 2000 annually

2007-USP/NFUSP 30 – NF 25 : 

2007-USP/NFUSP 30 – NF 25 This section provides background information on the United States Pharmacopeial Convention USP-30 and the 25 edition of the National Formulary (NF 25 USP–NF is published in continuing pursuit of the mission of USP promotes the public health and benefits practitioners and patients by disseminating authoritative standards and information developed by its volunteers for medicines other health care technologies, and related practices used to maintain and improve health and promote optimal health care delivery

2007-USP/NFUSP 30 – NF 25 : 

2007-USP/NFUSP 30 – NF 25 the United States Pharmacopeia – National Formulary and its Supplements will become official six months after being released to the public. The USP – NF, which is released on November 1 of each year, will become official on May 1 of the Next year

2007-USP/NFUSP 30 – NF 25 : 

2007-USP/NFUSP 30 – NF 25 Official Date May 1, 2007 Release Date Nov. 1, 2006 Official Until May 1, 2008 (except as superseded by Supplements, IRAs, and Revision Bulletins First Supplement Release Date: Feb. 1, 2007 Official Date: Aug. 1 2007 Official Until May 1, 2008 (except as superseded by Second Supplement, IRAs, and Revision Bulletins )

2007-USP/NFUSP 30 – NF 25 : 

2007-USP/NFUSP 30 – NF 25 Second Supplement Release Date: June 1 2007 Official Date: Dec. 1 2007 Official Until May 1, 2008 (except as superseded by Second Supplement, IRAs, and Revision Bulletins ) Note:- USP and the NF were recognized in the Federal Food and Drugs Act of 1906 and again in the Federal Food, Drug, and Cosmetic Act of 1938. In 1975, USP acquired the National Formulary (NF) and began publishing both compendia in a single volume, titled USP –NF. Today, USP continues to develop USP-NF through the work of the Council of Experts into compendia that provide standards for articles based on advances in analytical and metrological science. As these and allied sciences evolve, so do USP and NF

2007-USP/NF Contains : 

2007-USP/NF Contains Monographs Approximately 4,100 General Tests and Assays More than 200 (General Chapters numbered 1,000 and below) General Information Chapters Numbered above 1,000. General Chapters provide frequently cited procedures,sometimes with acceptance criteria, in order to compile into one location repetitive information that appears in many monographs. New and revised monographs and General Chapters and obsolete matter deleted from this edition are indicated.

2007-USP/NF printed as a three-volume set, due to the increase in content & Two Supplements. : 

2007-USP/NF printed as a three-volume set, due to the increase in content & Two Supplements. *Volume 1  Content Front Matter, USP/NF General Notices, General Chapters, Dietary Supplement Chapters, Reagents Reference Tables, Dietary Supplement Monographs also include the full index. Monographs for drug substances and preparations. *Volume 2  Content : USP Monographs A –To- L &General Notices and the Guide to General Chapters also include the full index. Monographs for drug substances and preparations. *Volume 2  Content : USP Monographs M –To- Z and include the full index. Monographs for drug substances and preparations.

2007-USP/NF Contains : 

2007-USP/NF Contains Supplements —One The First Supplement to USP 30 – NF 25 will be published in February 2007 and will become official in August 2007. Supplements —Two The Second Supplement to USP 30 – NF 25 will be published in June 2007 and will become official in December 2007. Users of USP print products must retain Supplements and subscriptions to Pharmacopeial Forum (PF) in order to have up-to-date information. The Index in each Supplement is cumulative and includes citations to the annual revision and, for the Second Supplement, Citations to the First Supplement of the USP – NF The contents of the two Supplements are integrated into the annual edition of the following year, along with new official revisions that have been adopted since the Second Supplement to the previous compendia.

British Pharmacopoeia SOCIAL SERVICES AND PUBLIC SAFETY : 

British Pharmacopoeia SOCIAL SERVICES AND PUBLIC SAFETY THIS PUBLICATION IS A VALUE ADDED PRODUCT. The Commission on Human Medicines wishes to record its appreciation of the services of all those who have contributed to this important work.

BPMission and Preface : 

BPMission and Preface The British Pharmacopoeia contributes significantly to the overall control of the quality of medicinal products by providing an authoritative statement of the quality that a product, material or article is expected to meet at any time during its period of use. The Pharmacopoeial standards, which are publicly available and legally enforceable, are designed to complement and assist the licensing and inspection processes and are part of the system for safeguarding purchasers and users of medicinal products. The Commission on Human Medicines wishes to record its appreciation of the services of all those who have contributed to this important work.

2007 British Pharmacopoeia : 

2007 British Pharmacopoeia the British Pharmacopoeia and its Supplements will become official six months after being released to the public. The BP, which is released on August 2006 , will become official on 1 January 2007of the Next year

2007 British Pharmacopoeia : 

2007 British Pharmacopoeia Official Date  1 January 2007 Release Date  August 2006 Official Until Next Edition

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