Skip Navigation LinksEBook Details

The Regulation of Drugs in Canada

The Regulation of Drugs in Canada
Author: Nessim Abu-Zahra; Simon Carvalho; David Edwards
Price: $125.00
ISBN-10: 1552216667
ISBN-13: 9781552216668
Get It!:
Format: PDF
Delivery: BibliU Reader
Duration: Lifetime

Note:
Copy Selections To Clipboard: User can copy content to the clipboard with the following restriction: Initially allowance of 10 copy selections. Another copy selection allowed every Day. To a maximum of 100 total copy selections.
Printing Pages: User can print pages with the following restriction: Initially allowance of 10 pages. Another page allowed every Day. To a maximum of 100 total pages.

Description

The Regulation of Drugs in Canada: The?Food and Drugs Act?and Related Intellectual Property Regimes provides an overview of the laws in Canada that govern the manufacture and sale of drugs that are subject to the?Food and Drugs Act, including?pharmaceuticals, vaccines, and natural health products.?Among the laws that are discussed are the new regulatory pathways that were made in response to the COVID-19 pandemic. This book also describes the intellectual property framework that applies to drugs and explains the impact this framework has on the drug approval process, as well as its unique objective:?to encourage innovation and incentivize bringing new therapeutic options to market. Authors Simon Carvalho and Nessim Abu-Zahra explain how this framework regulates the competition between “brand-name manufacturers” who are the first to bring a drug to market and obtain patents and other intellectual property, and “generic” or “biosimilar” manufacturers, who manufacture and sell copies of brand-name products.