wyszukanych pozycji: 41
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Statistical Design and Analysis in Pharmaceutical Science: Validation, Process Controls, and Stability
ISBN: 9780367401870 / Angielski / Miękka / 2019 / 580 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. |
cena:
315,36 zł |
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Design and Analysis of Bioavailability and Bioequivalence Studies
ISBN: 9781032477770 / Angielski / Miękka / 2023 / 756 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. Taking into account the regulatory and scientific developments that have occurred since its predecessor, this third edition presents a comprehensive summary of the ever-expanding literature and research in the field. It focuses on regulatory requirements, current scientific and practical issues, and the statistical methodology of designing and a
Taking into account the regulatory and scientific developments that have occurred since its predecessor, this third edition presents a comprehensive s...
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cena:
223,79 zł |
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Design and Analysis of Animal Studies in Pharmaceutical Development
ISBN: 9780367579388 / Angielski / Miękka / 2020 / 408 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. |
cena:
233,96 zł |
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Frailty Models in Survival Analysis
ISBN: 9781420073881 / Angielski / Twarda / 2010 / 324 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. The concept of frailty offers a convenient way to introduce unobserved heterogeneity and associations into models for survival data. In its simplest form, frailty is an unobserved random proportionality factor that modifies the hazard function of an individual or a group of related individuals. Frailty Models in Survival Analysis presents a comprehensive overview of the fundamental approaches in the area of frailty models. The book extensively explores how univariate frailty models can represent unobserved heterogeneity. It also emphasizes correlated frailty... The concept of frailty offers a convenient way to introduce unobserved heterogeneity and associations into models for survival data. In its simples... |
cena:
788,53 zł |
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Statistics in Drug Research: Methodologies and Recent Developments
ISBN: 9780367396336 / Angielski / Miękka / 2019 / 384 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. |
cena:
315,36 zł |
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Handbook of Adaptive Designs in Pharmaceutical and Clinical Development
ISBN: 9780367577117 / Angielski / Miękka / 2020 / 496 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. |
cena:
233,96 zł |
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Adaptive Design Methods in Clinical Trials
ISBN: 9781032477602 / Angielski / Miękka / 2023 / 374 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. This second edition reflects recent developments and regulatory positions on the use of adaptive designs in clinical trials. It unifies the vast and continuously growing literature and research activities on regulatory requirements, scientific and practical issues, and statistical methodology. This edition significantly updates the chapters on p
This second edition reflects recent developments and regulatory positions on the use of adaptive designs in clinical trials. It unifies the vast and c...
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cena:
223,79 zł |
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Translational Medicine: Strategies and Statistical Methods
ISBN: 9780367386177 / Angielski / Miękka / 2019 / 224 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. |
cena:
315,36 zł |
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Methodologies in Biosimilar Product Development
ISBN: 9780367896348 / Angielski / Twarda / 2021 / 380 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. |
cena:
941,15 zł |
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Handbook of Adaptive Designs in Pharmaceutical and Clinical Development
ISBN: 9781439810163 / Angielski / Twarda / 2010 / 496 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. In response to the US FDA s Critical Path Initiative, innovative adaptive designs are being used more and more in clinical trials due to their flexibility and efficiency, especially during early phase development. Handbook of Adaptive Designs in Pharmaceutical and Clinical Development provides a comprehensive and unified presentation of the principles and latest statistical methodologies used when modifying trial procedures based on accrued data of ongoing clinical trials. The book also gives a well-balanced summary of current regulatory perspectives. ...In response to the US FDA s Critical Path Initiative, innovative adaptive designs are being used more and more in clinical trials due to t... |
cena:
788,53 zł |
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Statistical Design and Analysis in Pharmaceutical Science : Validation, Process Controls, and Stability
ISBN: 9780824793364 / Angielski / Twarda / 1995 / 580 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. Offers a unified presentation of statistical designs and methods of analysis for all stages of pharmaceutical development, emphasizing biopharmaceutical applications and demonstrating statistical techniques with real-world examples.
Offers a unified presentation of statistical designs and methods of analysis for all stages of pharmaceutical development, emphasizing biopharmaceutic...
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cena:
686,78 zł |
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Design and Analysis of Bioavailability and Bioequivalence Studies
ISBN: 9781584886686 / Angielski / Twarda / 2008 / 760 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. Preeminent Experts Update a Well-Respected Book Taking into account the regulatory and scientific developments that have occurred since the second edition, Design and Analysis of Bioavailability and Bioequivalence Studies, Third Edition provides a complete presentation of the latest progress of activities and results in bioavailability and bioequivalence on regulatory requirements, scientific and practical issues, and statistical methodology. New to the Third Edition
Preeminent Experts Update a Well-Respected Book Taking into account the regulatory and scientific developments that have occurred s... |
cena:
686,78 zł |
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Design and Analysis of Bridging Studies
ISBN: 9780367576745 / Angielski / Miękka / 2020 / 287 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. |
cena:
233,96 zł |
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Design and Analysis of Bridging Studies
ISBN: 9781439846346 / Angielski / Twarda / 2012 / 287 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. As the development of medicines has become more globalized, the geographic variations in the efficacy and safety of pharmaceutical products need to be addressed. To accelerate the product development process and shorten approval time, researchers are beginning to design multiregional trials that incorporate subjects from many countries around the world under the same protocol. Design and Analysis of Bridging Studies addresses the issues arising from bridging studies and multiregional clinical trials. For bridging studies, the book explores ethnic sensitivity, the... As the development of medicines has become more globalized, the geographic variations in the efficacy and safety of pharmaceutical products need to... |
cena:
559,60 zł |
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Sample Size Calculations in Clinical Research
ISBN: 9781138740983 / Angielski / Twarda / 2017 / 510 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. Like the well-regarded and bestselling second edition, Sample Size Calculations in Clinical Research, Third Edition, presents statistical procedures for performing sample size calculations during various phases of clinical research and development. This new edition will be updated throughout and will contain four entirely new chapters written especially for this edition.
Like the well-regarded and bestselling second edition, Sample Size Calculations in Clinical Research, Third Edition, presents statistical procedures f...
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cena:
686,78 zł |
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Sample Size Calculations in Clinical Research
ISBN: 9780367657765 / Angielski / Miękka / 2020 / 510 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. |
cena:
203,44 zł |
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Biosimilar Drug Product Development
ISBN: 9781498718790 / Angielski / Twarda / 2017 / 496 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. When a biological drug patent expires, alternative biosimilar products are developed. Biological drugs are different in many respects from drugs based on chemically synthesized small molecules. The development of biosimilar products is complicated and involves numerous considerations and steps. The assessment of biosimilarity and interchangeability is complicated and difficult. This book presents current issues for the development of biosimilars and gives detailed reviews of its various stages and contributing factors as well as relevant regulatory pathways and post-approval issues. When a biological drug patent expires, alternative biosimilar products are developed. Biological drugs are different in many respects from drugs ba... |
cena:
890,27 zł |
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Quantitative Methods for Hiv/AIDS Research
ISBN: 9781498734233 / Angielski / Twarda / 2017 / 290 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. Quantitative Methods in HIV/AIDS Research provides a comprehensive discussion of modern statistical approaches for the analysis of HIV/AIDS data. The first section focuses on statistical issues in clinical trials and epidemiology that are unique to or particularly challenging in HIV/AIDS research; the second section focuses on the analysis of laboratory data used for immune monitoring, biomarker discovery and vaccine development; the final section focuses on statistical issues in the mathematical modeling of HIV/AIDS pathogenesis, treatment and epidemiology. This book brings... Quantitative Methods in HIV/AIDS Research provides a comprehensive discussion of modern statistical approaches for the analysis of HIV/AIDS data. T... |
cena:
559,60 zł |
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Quantitative Methods for Hiv/AIDS Research
ISBN: 9780367573171 / Angielski / Miękka / 2020 / 290 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. |
cena:
223,79 zł |
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Statistics In the Pharmaceutical Industry
ISBN: 9781032477879 / Angielski / Miękka / 2023 / 496 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. The growth of the pharmaceutical industry over the past decade is astounding, but the impact of this growth on statistics is somewhat confusing. While software has made analysis easier and more efficient, regulatory bodies now demand deeper and more complex analyses, and pharmacogenetic/genomic studies serve up an entirely new set of challenges. For more than two decades, Statistics in the Pharmaceutical Industry has been the definitive guide to sorting through the challenges in the industry, and this Third Edition continues that tradition. Updated and expanded to reflect the most recent...
The growth of the pharmaceutical industry over the past decade is astounding, but the impact of this growth on statistics is somewhat confusing. While...
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cena:
223,79 zł |