Industrial Pharmacy Detailed Syllabus for Pharmaceutics / Pharmaceutical Technology M.Pharm first year second sem is covered here. This gives the details about credits, number of hours and other details along with reference books for the course.
The detailed syllabus for Industrial Pharmacy M.Pharm 2017-2018 (R17) first year second sem is as follows.
M.Pharm. I Year II Sem.
Course Objectives: The students shall learn the theory of unit operations, machinery, materials of constructions, qualification of equipments and its utility. The students shall also understand about the objectives and principles of GMP, TQM and effluent analysis and specifications. They also understand the regulatory basis for the validation of analytical methods related to solids, sterile and liquid dosage forms
Course Outcome: The students will explain the machinery involved in milling, mixing, filteration, drying and packing material constructions used in the production of pharmaceutical materials. They also learn salient features of GMP, TQM applicable in industry. They also understand the effluent treatments and prevent the pollution. They also should evaluate the validation of analytical methods and processes
UNIT I : Pharmaceutical unit operations: A detailed study involving machinery and theory of Pharmaceutical unit operations like milling, mixing, filtration, and drying.
UNIT II
- Materials of construction of pharmaceutical equipment and packaging materials: Study of the principles, production techniques in the large scale production of tablets, capsules, suspensions, liquid pharmaceuticals, ophthalmic products, and sterile products.
- Qualification of equipment (IQ, OQ, PQ)
UNIT III : Production management: Production organization, objectives and policies of good manufacturing
practices, layout of buildings, services, equipments and their maintenance, material management, handling and transportation, inventory management and control, production and planning control, Sales forecasting, budget and cost control, industrial and personal relationship. Total Quality Management (TQM)
UNIT IV : Effluent Testing and Treatment: Effluent analysis, specifications, and preventive measures water of pollution, solid pollution, air pollution, and sound pollution.
UNIT V : Validation: Regulatory basis, validation of analytical methods, and process, in solid dosage forms, sterile products, and liquid dosage forms.
TEXT BOOKS:
- The Theory and Practice of industrial Pharmacy by Leon Lachman, Herbert A. Lieberman.
- Good Manufacturing Practice for Pharmaceuticals by Sidney H. willig.
- Pharmaceutical Process validation by Robert A. Nash, Alfred H. Wachter.
- Modern Pharmaceutics by Gilbert S. Banker and Christopher T. Rhodes.
- Pharmaceutical production management, C. V. S. Subrahmanyam, Vallabh Prakash.
REFERENCE BOOKS:
- Unit operations of Chemical Engineering by Warren L. McCabe, Julian C. Smith, Peter Harriott.
- Remington’s Science and Practice of Pharmacy by A. Gennaro.
- Bentley’s Text book of Pharmaceutics by EA Rawlins.
- CGMP, H.P.P. Sharma
For all other M.Pharm 1st Year 2nd Sem syllabus go to JNTUH M.Pharm Pharmaceutics / Pharmaceutical Technology 1st Year 2nd Sem Course Structure for (R17) Batch.
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