A Comprehensive Guide for the Novice Researcher in Clinical Trials
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- Taschenbuch
- eBook ausgewählt
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Form:Einzelkauf Download
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Sprache:Englisch
153,99 €
inkl. gesetzl. MwSt.Beschreibung
Produktdetails
Format
ePUB 3
Kopierschutz
Nein
Family Sharing
Nein
Text-to-Speech
Ja
Erscheinungsdatum
18.05.2026
Herausgeber
Miltiadis D. Lytras + weitereVerlag
Elsevier Science & Techn.Seitenzahl
320 (Printausgabe)
Dateigröße
15173 KB
Sprache
Englisch
EAN
9780443277443
A Comprehensive Guide for Novice Researcher in Clinical Trials is a must-have resource for individuals embarking on the journey of clinical research. This book is tailored for beginners, offering a clear and structured introduction to the vital principles, methodologies, and skills required to design and conduct robust clinical trials. Spanning 13 chapters, it meticulously covers the entire clinical trial process, emphasizing Good Clinical Practice (GCP) standards. From foundational research concepts to advanced trial strategies, the guide empowers readers to confidently navigate the complexities of clinical trials and contribute meaningfully to the field of healthcare.In addition to its foundational content, the book addresses a variety of important topics, such as ethical considerations, regulatory compliance, and the development of trial protocols. It explores different trial designs, types of bias, and the historical evolution of clinical research. Practical sections on data management, monitoring, statistical analysis, and project management offer readers hands-on guidance for real-world application. Notably, the book includes a dedicated focus on regulatory affairs in Saudi Arabia, making it particularly valuable for health professionals in that region.
- Includes content that follows a stepwise format, making it easy for novice researchers to absorb complex conception
- Focuses on the ethical considerations and GCP standards essential for conducting clinical trials
- Provides detailed insights into the responsibilities of researchers, informed consent processes, and strategies for maintaining participant safety and data integrity
- Includes practical tools and templates for protocol development, data management, and trial monitoring
- Includes content that follows a stepwise format, making it easy for novice researchers to absorb complex conception
- Focuses on the ethical considerations and GCP standards essential for conducting clinical trials
- Provides detailed insights into the responsibilities of researchers, informed consent processes, and strategies for maintaining participant safety and data integrity
- Includes practical tools and templates for protocol development, data management, and trial monitoring
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