COs of the course “Quality Management and IPR ”
Describes Good manufacturing practices for quality product of pharmaceutical industries
CO1 Define GMP with respect to manufacture of drugs, Packaging material, Personnel, hygiene, sanitation, waste and disposal
CO2 Describe quality assurance for manufacturing of drug
CO3 Explain quality control of raw material, processes and finished products
CO4 Implement industrial safety aspects
CO5 Evaluate rational drug design and identify intellectual property rights- Teacher: Dr. Shailesh Waghmare