Navigating the regulatory landscape is essential for the successful development and commercialization of herbal medicines. This book provides a comprehensive overview of the regulatory aspects governing herbal medicines, covering guidelines and requirements set by major regulatory bodies such as the FDA, EMA, and WHO. It discusses processes for herbal product registration, quality assurance, safety evaluation, and efficacy documentation. Additionally, the book explores challenges in achieving regulatory compliance, including standardization, labeling, and marketing claims. Aimed at regulatory affairs professionals, pharmacognosists, and herbal product developers, it offers practical insights into ensuring herbal medicines meet regulatory standards and gain market approval.
Karen Moore specializes in the regulatory aspects of herbal medicines, ensuring compliance and safety in their dermatological use. Her research focuses on navigating the legal frameworks and quality standards for herbal dermatological products. Karen has authored numerous studies on the regulatory requirements for the approval and marketing of herbal skin care treatments. She also provides guidelines for clinicians and manufacturers to adhere to regulatory standards, promoting safe and compliant use of herbal medicines in dermatology.