The journey from drug discovery to market approval is a complex and highly regulated process. This book provides an in-depth examination of drug development, covering preclinical research, clinical trials, and regulatory frameworks. It highlights the role of agencies like the FDA and EMA in ensuring drug safety and efficacy. Designed for researchers, industry professionals, and regulatory specialists, this book offers a comprehensive guide to navigating the drug development landscape.
Mason Holmes is a distinguished dermatologist specializing in drug development and regulatory affairs within the field of dermatology. His research focuses on the processes involved in bringing new dermatological medications to market, including clinical trials, regulatory compliance, and approval pathways. Mason has published extensively on the challenges and best practices in dermatological drug development, emphasizing safety and efficacy standards. He has developed comprehensive regulatory strategies that streamline the drug approval process.