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Evaluating Clinical Research
  • Language: en
  • Pages: 158

Evaluating Clinical Research

This book aims to make the readers better informed and more critical consumers of clinical research. It will help the reader recognize the strengths and the weaknesses of scientific publications. In doing so, the reader will be able to distinguish patient-important and methodologically sound studies from those having limitations in design, conduct and interpretation. The text is basic and has no statistical formulas. Key take-home messages are listed at the end of each chapter. Cartoons make the text easier to read and generate a few laughs, and they underscore specific points, sometimes in a provocative way.

Data Monitoring in Clinical Trials
  • Language: en
  • Pages: 389

Data Monitoring in Clinical Trials

From the authors of "Fundamentals of Clinical Trials" which has sold over 15,000 copies world wide since its publication in 1998. No competition yet as the text does not focus on how to do clinical trials but on very specific situations that can be encountered during the process.

Fundamentals of Clinical Trials
  • Language: en
  • Pages: 361

Fundamentals of Clinical Trials

A complete guide on all aspects of the development, management and analysis of clinical research for young established clinical investigators across all disciplines of medicine. The new edition includes a chapter on Meta-analysis and revised information on data monitoring, subgroup analysis, quality of life, pilot studies and run-ins.

Fundamentals of Clinical Trials
  • Language: en
  • Pages: 563

Fundamentals of Clinical Trials

  • Type: Book
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  • Published: 2015-08-27
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  • Publisher: Springer

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 and expanded. Many contemporary clinical trial examples have been added. There is much new material on adverse events, adherence, issues in analysis, electronic data, data sharing and international trials. This book is intended for the clinical researcher who is interested in designing a clinical tri...

Adequacy of FDA to Assure the Safety of the Nation’s Drug Supply: Congressional Hearing
  • Language: en
  • Pages: 326
Fundamentals of Clinical Trials
  • Language: en
  • Pages: 445

Fundamentals of Clinical Trials

The clinical trial is “the most definitive tool for evaluation of the applicability of clinical research.” It represents “a key research activity with the potential to improve the quality of health care and control costs through careful comparison of alternative treatments” [1]. It has been called on many occasions, “the gold st- dard” against which all other clinical research is measured. Although many clinical trials are of high quality, a careful reader of the medical literature will notice that a large number have deficiencies in design, conduct, analysis, presentation, and/or interpretation of results. Improvements have occurred over the past few decades, but too many trials...

FDA Reform Legislation
  • Language: en
  • Pages: 466

FDA Reform Legislation

  • Categories: Law
  • Type: Book
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  • Published: 1996
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  • Publisher: Unknown

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Nomination of Andrew von Eschenbach and Paul DeCamp : hearing
  • Language: en
  • Pages: 188

Nomination of Andrew von Eschenbach and Paul DeCamp : hearing

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Nomination of Andrew Von Eschenbach and Paul DeCamp
  • Language: en
  • Pages: 160