Managing Clinical Trials (Responsibilities & Liabilities)

This book highlights the critical role of clinical trials in advancing medical knowledge and improving patient care. It outlines the importance of ethical considerations, regulatory requirements, and best practices in the conduct of clinical trials, emphasizing the collaborative efforts of various stakeholder's summarizes the key points of the book, reinforcing the importance of ethical and regulatory adherence, effective communication, and best practices in clinical trial management. It emphasizes the collective responsibility of stakeholders in advancing medical science responsibly and ethically. This comprehensive guide provides valuable insights for all stakeholders involved in clinical trials, aiming to enhance the integrity, efficiency, and ethical conduct of clinical research.

Autorentext
Dr. Mohammad Nadeem Khan is currently serving Clinical Research and Trails Manager of Department of Clinical Pharmacology, SAMC&PGI, Indore and doing Phase-1 to Phase-4 clinical research and trials. He is major research interest in Biopharmaceuticals, Molecular medicine, Proteomics, Biochemistry, Microbiology, Nutraceuticals and In-Silico.