Description
Basics of Clinical Trials is an authoritative reference that provides healthcare professionals and researchers with a thorough understanding of clinical trial design, conduct, and management. The book covers fundamental principles including study design types, patient recruitment and retention strategies, data collection methods, and statistical analysis approaches.
Written by Sandeep Kumar Gupta, this essential resource addresses regulatory compliance, ethical considerations, and quality assurance in clinical research. It explores both Phase I through Phase IV trials, examining how drugs move from laboratory testing to patient availability. The text includes practical guidance on protocol development, informed consent procedures, adverse event monitoring, and documentation requirements.
Ideal for medical students, research coordinators, clinical investigators, and pharmaceutical professionals, this book serves as both an educational tool and a practical reference for anyone involved in clinical trial operations and oversight.
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