Global Clinical Research Regulations: Guidelines for Ethical Drug Development and Global Compliance
| AUTHOR | Dr Raghavendra Kumar Gunda; Dr C Madhavi Latha; Dr Sk Farahan Subahan |
| PUBLISHER | Notion Press (10/14/2024) |
| PRODUCT TYPE | Paperback (Paperback) |
GLOBAL CLINICAL RESEARCH REGULATIONS
Guidelines for Ethical Drug Development and Global Compliance
Clinical research is a cornerstone of modern healthcare, driving the development of innovative treatments, vaccines, and medical devices. However, navigating the complex regulatory landscape across different countries presents significant challenges for researchers, sponsors, and regulatory bodies alike.
Global Clinical Research Regulations: Guidelines for Ethical Drug Development and Global Compliance provides a comprehensive guide to the global regulatory frameworks that govern clinical trials. It explores the critical ethical considerations and compliance standards necessary for conducting trials across borders.
This book delves into essential topics such as:
Ethical Principles in Global Research: Informed consent, participant protection, and safeguarding vulnerable populations.
Phase-Wise Drug Development: Detailed guidelines for Phase I-IV trials and post-marketing surveillance.
Multinational Regulatory Requirements: Insights into the FDA, EMA, and other global agencies' regulations, ensuring adherence to Good Clinical Practice (GCP).
GLOBAL CLINICAL RESEARCH REGULATIONS
Guidelines for Ethical Drug Development and Global Compliance
Clinical research is a cornerstone of modern healthcare, driving the development of innovative treatments, vaccines, and medical devices. However, navigating the complex regulatory landscape across different countries presents significant challenges for researchers, sponsors, and regulatory bodies alike.
Global Clinical Research Regulations: Guidelines for Ethical Drug Development and Global Compliance provides a comprehensive guide to the global regulatory frameworks that govern clinical trials. It explores the critical ethical considerations and compliance standards necessary for conducting trials across borders.
This book delves into essential topics such as:
Ethical Principles in Global Research: Informed consent, participant protection, and safeguarding vulnerable populations.
Phase-Wise Drug Development: Detailed guidelines for Phase I-IV trials and post-marketing surveillance.
Multinational Regulatory Requirements: Insights into the FDA, EMA, and other global agencies' regulations, ensuring adherence to Good Clinical Practice (GCP).