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