Modern Medicine
eBook - ePub

Modern Medicine

Biomedical Devices, Medical Gases, Radiopharmaceuticals, New Drug Discovery, Volume 2

  1. 380 pages
  2. English
  3. ePUB (mobile friendly)
  4. Available on iOS & Android
eBook - ePub

Modern Medicine

Biomedical Devices, Medical Gases, Radiopharmaceuticals, New Drug Discovery, Volume 2

About this book

Modern Medicine: Biomedical Devices, Medical Gases, Radiopharmaceuticals, New Drug Discovery, Volume 2 discusses the procedures of drug approval and regulatory requirements that must be met according to the United States Food and Drug Administration (FDA), the European Medical Agency (EMA), and the Central Drug Standard Control Organization (CDSCO). In the rapidly evolving landscape of modern medicine, groundbreaking innovations have emerged that are reshaping the way we approach healthcare. Modern Medicine delves into the cutting-edge realms of medical devices, medical gases, radiopharmaceuticals, and new drug discovery, offering a comprehensive exploration of these transformative fields that are revolutionizing patient care and medical practices.

  • Discover the future of healthcare technology, and uncover the intricate world of biomedical engineering, where state-of-the-art devices seamlessly merge with the human body to monitor, diagnose, and treat ailments
  • Dive deep into the utilization of medical gases for respiratory conditions, pain management, and even novel applications in regenerative medicine
  • Unravel the mysteries of radiopharmaceuticals, a fusion of molecular imaging and therapy that offers unprecedented insights into the inner workings of the human body
  • Embark on a journey through the intricate processes of drug discovery, where groundbreaking research and cutting-edge technologies are yielding therapies that were once deemed impossible

Modern Medicine is a must-read for medical professionals, researchers, students, and anyone intrigued by the remarkable intersection of science, technology, and patient well-being. Join us on a journey to the forefront of medical innovation, where the unimaginable becomes reality, and the future of healthcare takes shape before our eyes. The chapter on regulatory implications for the approval process in this book will be the most useful resource for researchers and students, particularly those with backgrounds in pharma, forensic medicine, regulatory affairs, or those who aspire to succeed in drug research. Additionally, the information contained in this volume of the book could be of great interest to researchers working in the pharmaceutical and health industries.

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Information

Publisher
CRC Press
Year
2024
Print ISBN
9781032503004
eBook ISBN
9781040018385

Table of contents

  1. Cover
  2. Half-Title
  3. Title
  4. Copyright
  5. Contents
  6. Acknowledgement
  7. Preface
  8. Author Biographies
  9. Disclaimer
  10. Chapter 17 New Drug or Investigational New Drug Applications’ (INDA) Approval Process with the Drugs and Cosmetics Act
  11. Chapter 18 Medical Device Rules and Enforcement
  12. Chapter 19 Schedule of Medical Device and Minimum Requirement of Approval
  13. Chapter 20 Approval and Registration Process of a Medical Device
  14. Chapter 21 Quality Assurance of Medical Devices Central Drugs Standard Control Organization (CDSCO), the United States Food and Drug Administration (US FDA), and European Union (EU) Regulations
  15. Chapter 22 Regulation in Practising Telemedicine at the Edge of Data Confidentiality and Medical Ethics
  16. Chapter 23 Compressed Medical Gases: Regulations and Quality Control
  17. Chapter 24 Regulation of Radiopharmaceuticals in the Preview of the Drugs and Cosmetics Act, 1940
  18. Chapter 25 Abbreviated New Drug Application (ANDA) or Generic Drug Approval Process
  19. Chapter 26 Biological Licence Application (BLA) Procedures
  20. Chapter 27 Regulatory Approval of Biosimilars Including Nucleic Acid-based Recombinant Products, Recombinant Therapeutic Enzymes, and Protein
  21. Chapter 28 Regulations of Biopharmaceuticals Using Living Microorganisms, Genetically Modified Foods, and Vaccine Development
  22. Chapter 29 Role of Institutional Biosafety Committee
  23. Chapter 30 Orphan Drugs and Regulatory Approval
  24. Chapter 31 Regulatory Approval Process of In-vitro Diagnostics
  25. Index

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Yes, you can access Modern Medicine by Pronobesh Chattopadhyay,Danswrang Goyary in PDF and/or ePUB format, as well as other popular books in Medicine & Radiology, Radiotherapy & Nuclear Medicine. We have over 1.5 million books available in our catalogue for you to explore.