About this document
M.Pharm in Drug Regulatory Affairs by Mehak Lubana is a document available to read on EtoBox.
The document outlines the syllabus for a Master of Pharmacy program focused on Drug Regulatory Affairs. The program will cover topics such as current good manufacturing practices, pharmaceutical validation, quality management systems, and pharmaceutical regulatory requirements. Specific topics include CGMP, drug development and approval processes, process validation, quality control, documentation requirements, and relevant laws and guidelines. Coursework will include both theoretical instruction and practi
- Author
- Mehak Lubana
- Language
- EN