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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…mehr

Produktbeschreibung
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.
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Autorenporträt
Doktor Mohammad Nadeem Khan w nastoqschee wremq rabotaet menedzherom po klinicheskim issledowaniqm i marshrutam w otdele klinicheskoj farmakologii SAMC&PGI, Indor, i prowodit klinicheskie issledowaniq i ispytaniq ot fazy 1 do fazy 4. Ego osnownye nauchnye interesy swqzany s biofarmacewtikoj, molekulqrnoj medicinoj, proteomikoj, biohimiej, mikrobiologiej, nutricewtikami i In-Silico.