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“ashok kumar peepliwal”

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  • Clinical Trial Project Management

    de Ashok Kumar Peepliwal ...
    Clinical Trial Project Management provides a detailed overview of how to conduct clinical trials, in an international context. The process of conducting clinical studies across nations is based on a set of regulatory regimes developed by respective regulatory agencies. The book focuses on clinical study protocol approval processes, Ethics Committee approval processes, clinical study feasibilities, ... Leer más

    $152.99 USD

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  • Health Informatics: Practical Guide, Seventh Edition

    de Robert E. Hoyt, William R. Hersh ...
    Health Informatics: Practical Guide focuses on the application of information technology in healthcare to improve individual and population health, education and research. The goal of the seventh edition is to stimulate and educate healthcare and IT professionals and students about the key topics in this rapidly changing field. Dr. William Hersh from Oregon Health & Science University is the co ... Leer más

    $28.99 USD

  • Clinical Research Coordinator Handbook, Fourth Edition

    de Deborah Norris ...
    In this fully revised and expanded fourth edition of the essential reference for clinical research coordinators, Deborrah Norris provides expanded coverage of CRC duties and regulatory requirements, including new sections on investigator responsibilities, data clarification, and adverse event reporting. The books five appendices include a directory of CRC resources, updated forms and checklists, ... Leer más

    $9.99 USD o gratis con Kobo Plus

  • Clinical Research Coordinator Handbook, 5th edition

    de Deborrah Norris ...
    “This extremely useful title is written for anyone planning to implement clinical trials at an institution. … the author has carefully detailed the types of forms, study records, and case report forms. … A powerful appendix and glossary of relevant terms help make this a needed book for any clinical trials office.”— Journal of Hospital LibrarianshipIn this fully revised and expanded fifth edition ... Leer más

    $9.99 USD o gratis con Kobo Plus

  • Health Informatics

    Practical Guide

    Edición de William Hersh ...
    Health informatics (also known as biomedical and health informatics or just plain informatics) is the field concerned with the optimal use of data and information, usually aided by technology, to improve individual health, healthcare, public health, and biomedical research. The goal of this book is to provide a comprehensive introduction to the major areas of the field, both for those who are just ... Leer más

    $25.19 USD

  • Clinical Trials Audit Preparation

    A Guide for Good Clinical Practice (GCP) Inspections

    de Vera Mihajlovic-Madzarevic ...
    A must-have guide for any professional in the drug manufacturing industryThe Good Clinical Practice (GCP) audit is a tedious but necessary exercise that assures that all parties do their job properly and in compliance with the applicable FDA code. Clinical Trials Audit Preparation demystifies the audit process for all parties involved, including clinical research sponsors, clinical investigators, ... Leer más

    $97.00 USD

  • Pharmacovigilance Medical Writing

    A Good Practice Guide

    de Justina Orleans-Lindsay ...
    Pharmacovigilance Medical Writing covers the preparation of pharmacovigilance documents for all stages of the drug development process (i.e. from clinical development through to applications for marketing authorisations to the post-marketing stage). For each document, the book presents a review of the regulatory framework that governs the content of the document, followed by practical guidance (e ... Leer más

    $51.00 USD

  • Drug Information: A Guide for Pharmacists, Seventh Edition

    de Patrick M. Malone, Meghan J. Malone, Benjamin A. Witt, David M. Peterson ...
    Everything pharmacists and pharmacy students need to know about drug information managementA Doody's Core Title for 2023, 2024 & 2026!Drug Information: A Guide for Pharmacists provides you with the tools you need to to research, interpret, evaluate, collate, and disseminate drug information in the most effective and efficient manner possible. This trusted resource addresses essential topics such ... Leer más

    $93.59 USD

  • Drug Information: A Guide for Pharmacists, Sixth Edition

    de Patrick M. Malone, Meghan J. Malone, Sharon K. Park ...
    The guide pharmacists and students turn to first for cutting-edge coverage of drug informationA Doody’s Core Title for 2021!The goal of Drug Information: A Guide for Pharmacists, Sixth Edition is to teach students and practitioners how to effectively research, interpret, evaluate, collate, and disseminate drug information in the most efficient and effective manner possible. Updated to reflect the ... Leer más

    $85.49 USD

  • A Clinical Trials Manual From The Duke Clinical Research Institute

    Lessons from a Horse Named Jim

    de Margaret Liu, Kate Davis ...
    "The publication of the second edition of this manual comes at an important juncture in the history of clinical research. As advances in information technology make it possible to link individuals and groups in diverse locations in jointly seeking the answers to pressing global health problems, it is critically important to remain vigilant about moral and ethical safeguards for every patient ... Leer más

    $80.00 USD

  • Real-World Evidence in Drug Development and Evaluation

    Edición de Harry Yang, Binbing Yu ...
    Series series Chapman & Hall/CRC Biostatistics Series
    Real-world evidence (RWE) has been at the forefront of pharmaceutical innovations. It plays an important role in transforming drug development from a process aimed at meeting regulatory expectations to an operating model that leverages data from disparate sources to aid business, regulatory, and healthcare decision making. Despite its many benefits, there is no single book systematically covering ... Leer más

    Antes $57.99 USD Ahora $51.99 USD

  • Regulatory Affairs in the Pharmaceutical Industry

    Edición de 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 ... Leer más

    $179.99 USD