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  • The Versailles Anomaly: A Bourbon Crown Prince Out of Time1

    by William Wang ...
    Series Book 1 - The Versailles Anomaly: A Bourbon Crown Prince Out of Time
    God,this is insane.I—a 21st-century Chinese kid—have been reincarnated into the Kingdom of France under the Bourbon dynasty.But here’s the realkicker:I’m the Crown Prince of France.The catch?The king right now is Louis XVI…and in just a few years,he’ll be guillotined.Surrounded by 18th-century French nobles who speak a language I barely grasp,dressed in silk and powdered wigs while my mind races ... Read more

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  • Dragon & Sorcerer :A Love Bound by Blood 1

    by William Wang ...
    Series Book 1 - Dragon & Sorcerer :A Love Bound by Blood
    Reborn and transported to a world akin to Dungeons & Dragons, a boy grows step-by-step into a legendary sorcerer—only to find himself entangled in a forbidden love for his own sister. This is no mere adventure: it’s a mortal’s defiance of deities, a journey from pawn to player on a cosmic chessboard. It’s the story of a Netherese scion reclaiming his fallen empire’s glory, set in the iconic ... Read more

    $0.99 CAD or Free with Kobo Plus

  • Master Protocol Clinical Trials for Evidence Generation

    Strategies, Designs, Operations, and Case Studies

    Series series Chapman & Hall/CRC Biostatistics Series
    Drug development is at a crossroads. As personalized medicine and targeted therapies expand, traditional clinical trial models have become too slow, costly, and inefficient. To meet the urgent need for faster, reliable evidence generation and decision making, researchers and regulators alike have turned to innovative trial designs. Among these, master protocols stand out as a transformative ... Read more

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  • Simultaneous Global New Drug Development

    Multi-Regional Clinical Trials after ICH E17

    Series series Chapman & Hall/CRC Biostatistics Series
    Global simultaneous development is becoming more necessary as the cost of developing medical products continues to grow. The strategy of using multiregional clinical trials (MRCTs) has become the preferred method for developing new medicines. Implementing the same protocol to include subjects from many geographical regions around the world, MRCTs can speed up the patient enrolment, thus resulting ... Read more

    $152.99 CAD

  • Quantitative Drug Safety and Benefit Risk Evaluation

    Practical and Cross-Disciplinary Approaches

    Series series Chapman & Hall/CRC Biostatistics Series
    Quantitative Methodologies and Process for Safety Monitoring and Ongoing Benefit Risk Evaluation provides a comprehensive coverage on safety monitoring methodologies, covering both global trends and regional initiatives. Pharmacovigilance has traditionally focused on the handling of individual adverse event reports however recently there had been a shift towards aggregate analysis to better ... Read more

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    Series series Mathematics and Statistics (R0)
    This is the fifth edition of a very successful textbook on clinical trials methodology, written by recognized leaders who have long and extensive experience in all areas of clinical trials. The three authors of the first four editions have been joined by two others who add great expertise. A chapter on regulatory issues has been included and the chapter on data monitoring has been split into two ... Read more

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  • Principles and Practice of Clinical Research

    The third edition of this innovative work again provides a unique perspective on the clinical discovery process by providing input from experts within the NIH on the principles and practice of clinical research. Molecular medicine, genomics, and proteomics have opened vast opportunities for translation of basic science observations to the bedside through clinical research. As an introductory ... Read more

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  • Textbook of Pharmacoepidemiology

    Textbook of Pharmacoepidemiology, Second Edition, provides an introduction to pharmacoepidemiology and the data sources, methods and applications used in clinical research, the pharmaceutical industryand regulatory agencies.Drawing upon the fifth edition of the authoritative reference, Pharmacoepidemiology, this new edition covers the key learning requirements of the discipline. The textbook ... Read more

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  • Real-World Evidence in Drug Development and Evaluation

    Edited by 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 ... Read more

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  • Principles and Practice of Clinical Research

    Principles and Practice of Clinical Research, Fourth Edition has been thoroughly revised to provide a comprehensive look at both the fundamental principles and expanding practice of clinical research. New to this edition of this highly regarded reference, authors have focused on examples that broadly reflect clinical research on a global scale while including a discussion of international ... Read more

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  • Principles and Practice of Clinical Trial Medicine

    Clinical trials are an important part of medicine and healthcare today, deciding which treatments we use to treat patients. Anyone involved in healthcare today must know the basics of running and interpreting clinical trial data. Written in an easy-to-understand style by authors who have considerable expertise and experience in both academia and industry, Principles and Practice of Clinical Trial ... Read more

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  • Clinical Trial Management – an Overview

    by Editor IJSMI ...
    Clinical Trials word became a buzz word during this pandemic situation. It played a crucial role in developing vaccine to fight the pandemic.Experts from different fields contribute to the development of vaccine which includes (not limited) clinical researchers, health care providers, pharmaceutical industry, data managers, biostatisticians, data scientist and clinical trial programmers. Data ... Read more

    $13.99 CAD or Free with Kobo Plus