Principles and Practices in Clinical Research
Description
This book comprehensively reviews fundamental principles, ethical considerations, regulatory frameworks, and emerging trends in clinical research. The introductory chapters explore the fundamentals of clinical research, its historical context, and the pivotal role of key stakeholders. The book explores regulatory frameworks in various regions, including the USA, EU countries, non-EU countries, and India. It also delves into the implementation of International Conference on Harmonization (ICH) guidelines, ensuring compliance and quality in clinical trials. It meticulously dissects ethical considerations, delving into historical breaches to underscore the paramount importance of ethical integrity. The chapters outline regulatory standards, emphasize data accuracy and confidentiality, and prepare researchers for regulatory inspections and audits. Moreover, the chapter provides a concise yet comprehensive guide to protocol development and statistical analysis in clinical research. From the inception of research protocols to the intricacies of statistical analysis, the book offers practical insights and methodologies crucial for conducting rigorous and ethically sound research. Moreover, it critically examines emerging trends, from the integration of digital health technologies to the burgeoning role of machine learning and artificial intelligence. This book is intended for researchers, healthcare professionals, and regulatory stakeholders.
Key Features:
- Provides an in-depth examination of the fundamental principles underlying clinical research
- Review regulatory frameworks across multiple regions including the USA, EU, non-EU countries, and India
- Discusses the importance of ethics in clinical research, the role of ethical committees, and the informed consent process
- Covers fundamental clinical research methods, including study design, protocol development, and statistical analysis
- Addresses cutting-edge trends and innovations within clinical research, including the application of machine learning and AI tools
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Persons
Nidhi Bharal, Ph.D., MAMS is an accomplished academician and clinical scientist serving as an Associate Professor in the Department of Translational and Clinical Research at Jamia Hamdard, New Delhi. She obtained her Ph.D. in Pharmacology from University College of Medical Sciences & GTB Hospital (Delhi University) and previously completed her M. Pharm and B. Pharm in Pharmacology and Pharmaceutical Sciences from Jamia Hamdard. With over 22 years of teaching and research experience, her expertise spans neuropharmacology exploring repurposed or indigenous drugs for the treatment of epilepsy and autism along with neuroinflammatory pathways. She has also worked on neuro behavioural changes due to pharmacotherapeutics in Diabetes and Cancer patients. Dr. Nidhi has made significant contributions through her work on cognitive and psychological impairments in chronic conditions such as diabetes and cancer, leveraging standardized neuropsychological tools, depression scales, and quality-of-life instruments to generate clinically actionable insights. Her experience extends across clinical trial operations, pharmacovigilance, pharmacoepidemiology, and translational research, and she has been actively involved in both medical and pharmacy education at undergraduate and postgraduate levels. A recipient of multiple awards for her research work presented in various National & International Conferences including Dr. Vinod Kumar Bhargava Award by National Academy of Medical Sciences. She has also received ICMR grants for her research work.
Anoop Kumar currently working as an Assistant Professor in the Department of Pharmacology, Delhi Institute of Pharmaceutical Education and Research (DIPSAR), Delhi Pharmaceutical Sciences & Research University (DPSRU), Govt of NCT of Delhi. He has more than 10 years of teaching and research experience in reputed organizations like Cipla Pharmaceutical Limited Baddi, Shanti Niketan College of Pharmacy, Mandi, Sun Pharmaceutical Industries Limited, Gurugram, Translational Health Science Institute (THSTI), Faridabad, ISF College of Pharmacy, Moga, Punjab and National Institute of Pharmaceutical Education and Research (NIPER), Raebareli. Recently, he has also been included in top 2% list of scientists released by Stanford. His current h-index is 31, and i10-index 79 with citations of 3767 with more than 100 research and review articles. His lab gets funding from various government bodies like DST SERB, ICMR, NIF, and IIT-Delhi. His research interests are in the following areas: 1) Drug repurposing 2) Meta-analysis of clinical trials 3) Network Pharmacology 4) Pharmacoeconomic studies 5) Signal analysis in Pharmacovigilance 6) Animal experimental studies.
Content
Chapter 1: Introduction to Clinical Research. Chapter 2: Historical Background. Chapter 3: Protocol in Clinical Research. Chapter 4: Diversity in Clinical Trials. Chapter 5: Clinical Trial Protocol: The Backbone of a Clinical Trial. Chapter 6: Informed consent in Health Research. Chapter 7: Case Report Form. Chapter 8: Study Designs used in Clinical Research. Chapter 9: Regulatory Frameworks in India. Chapter 10: Regulatory Frameworks in USA. Chapter 11: Placebo and Nocebo. Chapter 12: Role of Pharmacovigilance in Clinical Research. Chapter 13: Statistical Consideration in Clinical Research. Chapter 14: Emerging Trends and Innovations in Clinical Research.