Medical Device Regulations: A Complete Guide describes a brief review of various regulatory bodies of major developed and developing countries around the world. The book covers the registration procedures of medical devices for pharmaceutical regulatory organizations. Sections provide guidance on dealing with the ethical considerations of medical device development, compliance with patient confidentiality using information from medical devices, the interoperability between, and among devices outside of healthcare, and the dynamics of implementation of new devices to ensure patient safety.
The author brings forth relevant issues, challenges and demonstrates how management can foster increased clinical and non-clinical relations to enhance patient outcomes and the bottom-line by demystifying the regulatory impact on operational requirements.
Table of Contents
1. Introduction of medical devices2. Ethics of clinical trials of medical devices
3. Regulations for medical devices in the United States
4. Regulations of medical devices in Europe
5. Regulations of medical devices in ASEAN countries
6. Regulations of medical devices in Japan and China
7. Regulations of medical devices in Canada
8. Regulations of medical devices in India
9. Regulations of medical devices in Australia
10. Regulations of medical devices in GCC countries
11. Regulations of medical devices in Sri Lanka
12. Regulations of medical devices in Russia
