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

    de William Wang ...
    Series Libro 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 ... Leer más

    $8.99 USD o gratis con Kobo Plus

  • Dragon & Sorcerer :A Love Bound by Blood 1

    de William Wang ...
    Series Libro 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 ... Leer más

    Antes $8.99 USD Ahora $4.99 USD o gratis con Kobo Plus

  • 家庭法方程式

    澳大利亚家庭法,看似充满情绪与冲突,但在法庭上,它其实更像一套可以被计算的结构。在每一个家庭法案件中,法官都会围绕几个核心变量作出判断:贡献、调整、证据、可信度,以及子女的最佳利益。这些变量共同决定了案件的最终结果。本书将复杂的澳大利亚家庭法逻辑拆解为一套清晰的"家庭法方程式"。作者以近二十年的法律实务经验,从律师与案件管理者的角度,系统解释:• 财产分割中贡献与未来调整如何影响比例• 为什么证据质量会成倍放大或归零一个案件• 子女案件中"最佳利益"的真实运作方式• 法庭如何评估可信度与证据结构• 为什么有些案件可以谈判解决,而有些必须进入法庭本书不是法律教科书,而是一份实践指南。它帮助读者理解澳大利亚家庭法案件背后的运作逻辑,让人们在面对婚姻、分居或家庭纠纷时,能够更清楚地看懂规则、风险与选择。如果你想真正理解澳大利亚家庭法是如何运作的,这本书将为你提供一张清晰的地图。 ... Leer más

    $40.99 USD

  • 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 ... Leer más

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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 ... Leer más

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  • 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 ... Leer más

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    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 ... Leer más

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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 ... Leer más

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  • Textbook of Pharmacoepidemiology

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  • Real-World Evidence in Drug Development and Evaluation

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    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

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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 ... Leer más

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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 ... Leer más

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