Botanicals, which have been part of human food and medicine for thousands of years, are perceived as being safer than synthetic pharmaceuticals. The global botanical drug market was expected to reach $26.6 billion by 2017. In terms of FDA regulations, botanical drugs are no different from non-botanical products, having to meet the safety and effectiveness standards of a new drug in accordance. This book comprises a complete start-to-end process from drug-idea conception, to drug development process. Key Features: Provides a complete compendium for botanical drug products Describes what BDP is and how it differs from Pharma, Biopharma, and Nutraceuticals Compiles all critical regulatory steps in a variety of countries Discusses clinical trial management for BDP development and how it differs from conventional chemical-based drugs and biopharmaceutics
This book comprises a complete start-to-end process from drug-idea conception, to drug development process for botanical drug products.
Publisher
CRC Press
Publication Date
Dec 2020
ISBN
9780367732479
Pages
274 p.
Item Type
Book
Format
Paperback
Unavailable
This product is currently out of stock. Please check back later.