logo

EbookBell.com

Most ebook files are in PDF format, so you can easily read them using various software such as Foxit Reader or directly on the Google Chrome browser.
Some ebook files are released by publishers in other formats such as .awz, .mobi, .epub, .fb2, etc. You may need to install specific software to read these formats on mobile/PC, such as Calibre.

Please read the tutorial at this link:  https://ebookbell.com/faq 


We offer FREE conversion to the popular formats you request; however, this may take some time. Therefore, right after payment, please email us, and we will try to provide the service as quickly as possible.


For some exceptional file formats or broken links (if any), please refrain from opening any disputes. Instead, email us first, and we will try to assist within a maximum of 6 hours.

EbookBell Team

Medical Device Regulations A Complete Guide Aakash Deep

  • SKU: BELL-50483678
Medical Device Regulations A Complete Guide Aakash Deep
$ 31.00 $ 45.00 (-31%)

5.0

50 reviews

Medical Device Regulations A Complete Guide Aakash Deep instant download after payment.

Publisher: Elsevier
File Extension: PDF
File size: 7.03 MB
Pages: 186
Author: Aakash Deep
ISBN: 9780323911269, 9780323911276, 0323911269, 0323911277
Language: English
Year: 2022

Product desciption

Medical Device Regulations A Complete Guide Aakash Deep by Aakash Deep 9780323911269, 9780323911276, 0323911269, 0323911277 instant download after payment.

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. Provides clear information on regulatory pathways for the design and commercialization of Medical Devices in different countries Explains the difference between standards and mandatory regulations for each region, along with discussions of regulations from USFDA (USA), CDSCO (India), EMEA (European Union), SFDA (China) and PMDA (Japan) Compiles regulations for medical devices and pharmaceuticals worldwide, helping readers create globally compliant products

Related Products