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« vikesh kumar shukla »

1-12 sur 12 résultats pour « vikesh kumar shukla »
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  • Understanding Pharmaceutical Standards and Regulations

    Insights Towards Best Practice

    Modifié par Navneet Sharma, Vikesh Kumar Shukla, Sandeep Arora ...
    This unique resource provides a comprehensive guide to the evolving regulations and standards which govern the international pharmaceutical industry. Featuring clear explanations of the latest regulations, as well as insights and strategies to maintain compliance, the book covers the key principles of best-practice for laboratory research, manufacturing, and distribution. It also offers strategies ... En savoir plus

    $122.99 CAD

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  • The Combination Products Handbook

    A Practical Guide for Combination Products and Other Combined Use Systems

    Modifié par Susan Neadle ...
    Combination products are therapeutic and diagnostic products that combine drugs, devices, and/or biological products. According to the US Food and Drug Administration (FDA), “a combination product is one composed of any combination of a drug and a device; a biological product and a device; a drug and a biological product; or a drug, device and a biological product.” Examples include prefilled ... En savoir plus

    $114.99 CAD

  • Logistics Operations and Management

    Concepts and Models

    Modifié par Reza Farahani, Shabnam Rezapour, Laleh Kardar ...
    This book provides a comprehensive overview of how to strategically manage the movement and storage of products or materials from any point in the manufacturing process to customer fulfillment. Topics covered include important tools for strategic decision making, transport, packaging, warehousing, retailing, customer services and future trends. - An introduction to logistics - Provides practical ... En savoir plus

    $132.99 CAD

  • Medical Product Regulatory Affairs

    Pharmaceuticals, Diagnostics, Medical Devices

    par John J. Tobin, Gary Walsh ...
    Written in a clear and concise style by an experienced author, this attractively-priced book covers regulatory affairs in all major global markets for pharmaceuticals and medical devices, making it the most comprehensive in its field.Following a look at drug development, complete sections are devoted to national and EU regulatory issues, manufacturing license application and retention, and ... En savoir plus

    $116.99 CAD

  • Current Good Manufacturing Practices (cGMP) for Pharmaceutical Products

    par Chandrasekhar Panda ...
    This Book contains 11 Modules of Current Good Manufacturing Practices (cGMP) requirements for pharmaceutical industry which will be very useful for job seekers in Pharma sector, Beginners and Learners of a Pharmaceutical industry and Pharmacy Students. It is a must-read book for every students aspiring for Placement in any pharmaceutical industry ... En savoir plus

    $10.99 CAD ou Gratuit avec Kobo Plus

  • Regulatory Aspects of Pharmaceutical Quality System

    Brief Introduction

    par Arun Kumar Pandey ...
    If you're a B. Pharm or M. Pharm student seeking a comprehensive yet concise guide to the regulatory aspects of pharmaceutical quality systems, look no further than Regulatory Aspects of Pharmaceutical Quality System – Brief Introduction. While other textbooks on quality assurance cover a variety of topics to varying degrees of depth, this book provides a unified approach that is both insightful ... En savoir plus

    $82.99 CAD ou Gratuit avec Kobo Plus

  • Regulatory Affairs in the Pharmaceutical Industry

    Modifié par Javed Ali, Sanjula Baboota ...
    Regulatory Affairs in the Pharmaceutical Industry is a comprehensive reference that compiles all the information available pertaining to regulatory procedures currently followed by the pharmaceutical industry. Designed to impart advanced knowledge and skills required to learn the various concepts of regulatory affairs, the content covers new drugs, generic drugs and their development, regulatory ... En savoir plus

    $176.99 CAD

  • The ASQ Certified Medical Device Auditor Handbook

    Modifié par Scott A. Laman ...
    The ASQ Certified Medical Device Auditor Handbook (formerly The Biomedical Quality Auditor Handbook) was developed by the ASQ Medical Device Division (formerly Biomedical Division) in support of its mission to promote the awareness and use of quality principles, concepts, and technologies in the medical device community. It principally serves as a resource to candidates preparing for the Certified ... En savoir plus

    $164.99 CAD

  • Good Clinical Practice eRegs & Guides For Your Reference Book 3

    par FDA, Biopharma Advantage Consulting L.L.C., eRegs And Guides a Biopharma Advantage Consulting L.L.C. ...
    Collections Livre 3 - Good Clinical Practice eRegs & Guides For Your Reference
    In this ebook you will find the following guidance documents: ICH Q8 Pharmaceutical Development ICH Q9 Quality Risk Management ICH Q10 Pharmaceutical Quality System ... En savoir plus

    $10.41 CAD

  • Medical Devices

    Regulations, Standards and Practices

    par Seeram Ramakrishna, Lingling Tian, Charlene Wang, Susan Liao, Wee Eong Teo ...
    Collections series Woodhead Publishing Series in Biomaterials
    Medical Devices and Regulations: Standards and Practices will shed light on the importance of regulations and standards among all stakeholders, bioengineering designers, biomaterial scientists and researchers to enable development of future medical devices. Based on the authors' practical experience, this book provides a concise, practical guide on key issues and processes in developing new ... En savoir plus

    $190.99 CAD

  • Data Integrity in Pharmaceutical and Medical Devices Regulation Operations

    Best Practices Guide to Electronic Records Compliance

    par Orlando Lopez ...
    Data integrity is fundamental in a pharmaceutical and medical devices quality system. This book provides practical information to enable compliance with data integrity, while highlighting and efficiently integrating worldwide regulation into the subject. The ideas presented in this book are based on many years’ experience in regulated industries in various computer systems development, maintenance ... En savoir plus

    $68.99 CAD

  • Risk Management Applications in Pharmaceutical and Biopharmaceutical Manufacturing

    Modifié par Hamid Mollah, Harold Baseman, Mike Long ...
    Collections Livre 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 ... En savoir plus

    $163.99 CAD