Course Description

• Orientation and overview of the Pharmaceuticals industry
• Managing Environmental Health and Safety Compliance 
• Application of Chemistry, Quality and Engineering Concepts in Manufacturing of Drugs
• cGMP for Production Personnel
• Standard Operating procedure - Preparation to Implementation
• Fundamentals of Clean Room Behaviour
• Manufacturing Process of Non-Sterile API and Drug Product (Including WPU and Packaging)
• Manufacturing Batch Record Review
• Developing CAPA Strategy in Pharma Manufacturing
• Manufacturing Quality Management
• GDP and Data Integrity (DI) for Production Personnel
• Change Control Process
• Process Validation for Production Personnel (including cleaning validation)
• Managing waste Disposal
• Audit Preparation for Production Personnel
• Professional Skills for Production Personnel 
  

   

  ELIGIBILITY: Graduates (B.Sc. / B. Pharm.) to Post Graduates (M.Sc. / M. Pharm.) in the field of Life Sciences and Pharmacy.