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“pp sharma”

Showing 1 - 12 of 12 results for “pp sharma”
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  • Validation in Pharmaceutical Industry

    by P.P. Sharma ...
    The first edition of this book was well received by the pharmaceutical industry and pharmacy education institutions. Over the years, since this book was published, there have been some changes e.g. acceptance limits in media fill trials, acceptance limits in cleaning validation. Thus, there was a need for review of this book.In the first edition, process validation, in general, was discussed and ... Read more

    $100.00 USD or Free with Kobo Plus

  • How to Practice GLP

    3rd EDITION

    by Sharma P P ...
    Like GMP, GLP also originated in the United States of America. US FDA had observed in some cases that studies submitted in support of safety of regulated products had not been conducted in acceptable manner. In view of this, GLP guidelines were incorporated under the Code of Federal Regulations (21CFR 58) in late seventies. Based on these guidelines a group of countries known as Organization for ... Read more

    $100.00 USD or Free with Kobo Plus

  • Drug Information about Commonly Used Drugs

    by P.P. Sharma ...
    Drug information is something that is needed by all pharma professionals whether in practice, industry, pharmacy education or regulatory. Drug information in this title has been compiled based on their use in disorders of different body systems like gastro-intestinal tract (GIT), respiratory tract, cardio-vascular system. In the introductory section of each part, there is general discussion on ... Read more

    $50.00 USD or Free with Kobo Plus

  • Stability Studies of Pharmaceutical & Cosmetic Products

    by P.P. Sharma ...
    The purpose of stability testing is to provide evidence on how the quality of an active pharmaceutical ingredient or medicinal product varies with time under the influence of a variety of environmental factors such as temperature, humidity, and light, and to establish a re-test period for the active pharmaceutical ingredient or a shelf life for the medicinal product and recommended storage ... Read more

    $75.00 USD or Free with Kobo Plus

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  • Process Architecture in Biomanufacturing Facility Design

    Edited by Jeffery Odum, Michael C. Flickinger ...
    Essential information for architects, designers, engineers, equipment suppliers, and other professionals who are working in or entering the biopharmaceutical manufacturing fieldBiomanufacturing facilities that are designed and built today are radically different than in the past. The vital information and knowledge needed to design and construct these increasingly sophisticated biopharmaceutical ... Read more

    $160.00 USD

  • Pharmaceutical Quality by Design

    A Practical Approach

    Edited by Walkiria S. Schlindwein, Mark Gibson ...
    Series series Advances in Pharmaceutical Technology
    A practical guide to Quality by Design for pharmaceutical product developmentPharmaceutical Quality by Design: A Practical Approach outlines a new and proven approach to pharmaceutical product development which is now being rolled out across the pharmaceutical industry internationally. Written by experts in the field, the text explores the QbD approach to product development. This innovative ... Read more

    $90.00 USD

  • Handbook of Validation in Pharmaceutical Processes, Fourth Edition

    Edited by James Agalloco, Phil DeSantis, Anthony Grilli, Anthony Pavell ...
    Revised to reflect significant advances in pharmaceutical production and regulatory expectations, Handbook of Validation in Pharmaceutical Processes, Fourth Edition examines and blueprints every step of the validation process needed to remain compliant and competitive. This book blends the use of theoretical knowledge with recent technological advancements to achieve applied practical solutions. ... Read more

    $66.99 USD

  • Essential Elements for a GMP Analytical Chemistry Department

    by Thomas Catalano ...
    Series series Biomedical and Life Sciences (R0)
    Essential Elements for a GMP Analytical Chemistry Department is a systematic approach to understanding the essential elements required for a successful GMP Analytical Department to function as an efficient and effective organization. It describes in detail a department structure which allows for the necessary processes to become available to all its personnel in a way where there is a free flow of ... Read more

    $143.09 USD

  • Improving Traceability in Food Processing and Distribution

    Edited by I Smith, A Furness ...
    Series series Woodhead Publishing Series in Food Science, Technology and Nutrition
    In the light of recent legislation and a number of food safety incidents, traceability of food products back from the consumer to the very beginning of the supply chain has never been so important. This important book describes key components of traceability systems and how food manufacturers can manage them effectively.After an introductory chapter on the nature of traceability systems, the first ... Read more

    $229.49 USD

  • Risk Management Applications in Pharmaceutical and Biopharmaceutical Manufacturing

    Edited by Hamid Mollah, Harold Baseman, Mike Long ...
    Series Book 4 - Wiley Series in Biotechnology and Bioengineering
    Sets forth tested and proven risk management practices in drug manufacturingRisk management is essential for safe and efficient pharmaceutical and biopharmaceutical manufacturing, control, and distribution. With this book as their guide, readers involved in all facets of drug manufacturing have a single, expertly written, and organized resource to guide them through all facets of risk management ... Read more

    $121.00 USD

  • ICH Quality Guidelines

    An Implementation Guide

    Edited by David Elder, Raymond W. Nims, Andrew Teasdale ...
    Examining the implications and practical implementation of multi-disciplinary International Conference on Harmonization (ICH) topics, this book gives an integrated view of how the guidelines inform drug development strategic planning and decision-making.• Addresses a consistent need for interpretation, training, and implementation examples of ICH guidelines via case studies• Offers a primary ... Read more

    $309.00 USD

  • Practical Approaches to Method Validation and Essential Instrument Qualification

    Edited by Chung Chow Chan, Herman Lam, Xue-Ming Zhang ...
    Practical approaches to ensure that analytical methods and instruments meet GMP standards and requirementsComplementing the authors' first book, Analytical Method Validation and Instrument Performance Verification, this new volume provides coverage of more advanced topics, focusing on additional and supplemental methods, instruments, and electronic systems that are used in pharmaceutical, ... Read more

    $108.00 USD