Industrial Pharmacy department was established in the year 2010. IP is a discipline of Pharmacy which deals with the formulation and development of old or new drug molecule into dosage form to provide safe, effective treatment to patient. Industrial pharmacists are responsible for quality control, using the latest technologies to research drug compounds, conduct trials to test medications for safety, and develop new drugs that save lives. The Master of Science program in Pharmaceutics with Specialization in Industrial Pharmacy prepares students for careers in the pharmaceutical manufacturing industry and for entry into Ph.D. programs in pharmaceutical sciences and other related fields.
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Career opportunities: |
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Mr Sravan Kumar Aligeti, Associate Professor, Department of Industrial Pharmacy. A well-known scholar, investigator, and expert in the pharmacy area. He has fifteen years of varied experience in both teaching and research. His research efforts have resulted in six papers being published in national and international journals, as well as participation in two international and twenty national conferences.
Vision
Our vision is to be internationally and nationally recognize as a centre of excellence in pharmaceutics and drug delivery, as distinguished by our innovative work in research and education
Mission
| S.No | Name of the Faculty | Designation | Qualification | Experience | PCI Reg.No. / JNTUH ID | Photo |
|---|---|---|---|---|---|---|
| 1 | Mr. Sravan Kumar Aligeti | Professor | M.Pharm., (Ph.D) | 15 | 3026-150411-105153 | |
| 2 | Mr.G.KoteshwarRao | Professor | M.Pharmacy (Pharmaceutics) | 15 | 4038-150409-131811 |  |
| 3 | Mrs.Rekhabai Thakur | Professor | M.Pharmacy (Pharmaceutics) | 10 | 2188-150522-162743 |
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| 4 | Mr.R.Raj Kumar | Professor | M.Pharmacy (Industrial Pharmacy) | 7 | 9202-190219-151917 |  |
| INDUSTRIAL PHARMACY I-Year I-semester | |||
| Course | Course Code | Course Outcome Number | Course Outcome |
| ADVANCED PHYSICAL PHARMACEUTICS | 6608AA | Upon completion of the course student will be able to | |
| 1 | know particle size analysis method, solid dispersion, physics of tablets, polymer classification and its applications, |
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| 2 | know the factors affecting the dissolution and solubility in related to invitro/invivo correlations |
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| 3 | know the stability calculations, shelf life calculations and accelerated stability studies. |
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| 4 | know the rheology, absorptionrelated to liquids and semi-solid dosage forms. | ||
| Course | Course Code | Course Outcome Number | Course Outcome |
| PHARMACEUTICAL FORMULATION DEVELOPMENT | 6608AB | Upon completion of the course student will be able to | |
| 1 | The Preformulation studies | ||
| 2 | The Pharmaceutical unit operations | ||
| 3 | Different machinery used for various steps in manufacture of various dosage forms. | ||
| 4 | Formulation and evaluation of hard and soft gelatin capsules and their advantages over other | ||
| Course | Course Code | Course Outcome Number | Course Outcome |
| DRUG REGULATORY AFFAIRS | 6608AD | Upon completion of the course student will be able to | |
| 1 | Students will come to know the different competent regulatory authorities globally. | ||
| 2 | Students be aware of technical aspects pertaining to the marketing authoritization application | ||
| 3 | The regulatory guidelines and directions framed by the regulatory authorities will be helpful to place the drug products in market for marketing approvals |
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| Course | Course Code | Course Outcome Number | Course Outcome |
| STABILITY OF DRUGS AND DOSAGE FORMS | 6608AH | Upon completion of the course student will be able to | |
| 1 | describe the evaluation of stability of solutions, solids andformulations against adverse conditions. | ||
| 2 | suggest the measures to retain stability and storage conditions for retaining the efficacy of the products |
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| 3 | Drug decomposition mechanisms | ||
| Course | Course Code | Course Outcome Number | Course Outcome |
| RESEARCH METHODOLOGY AND IPR | 6608AJ | Upon completion of the course student will be able to | |
| 1 | Understand research problem formulation. | ||
| 2 | Analyze research related information | ||
| 3 | Follow research ethics | ||
| 4 | Understand that today’s world is controlled by Computer, Information Technology, but | ||
| 5 | Understanding that when IPR would take such important place in growth of individuals &nation, it is needless to emphasis the need of information about Intellectual Property Right tobe promoted among students in general & engineering in particular | ||
| 6 | Understand that IPR protection provides an incentive to inventors for further research workand investment in R & D, which leads to creation of new and better products, and in turnbrings about, economic growth and social benefits | ||
| Course | Course Code | Course Outcome Number | Course Outcome |
| VALUE EDUCATION | 6608AP | Upon completion of the course student will be able to | |
| 1 | Knowledge of self-development | ||
| 2 | Learn the importance of Human values | ||
| 3 | Developing the overall personality | ||
| Course | Course Code | Course Outcome Number | Course Outcome |
| PHARMACEUTICAL FORMULATION DEVELOPMENT LAB | 660802 | Upon completion of the course student will be able to | |
| 1 | the preformulation studies of solid dosage forms. | ||
| 2 | Accelerated stability testing of different tablets | ||
| 3 | To study pharmacokinetic models, to determine similarity factors | ||
| 4 | the effect of compressional force on tablet disintegration time,study the micromeritic properties of powders and granules | ||
| 5 | the effect of particle size on dissolution of tablets,the effect of binders on dissolution of tablets | ||
| Course | Course Code | Course Outcome Number | Course Outcome |
| ADVANCED PHYSICAL PHARMACEUTICS LAB | 660801 | Upon completion of the course student will be able to | |
| 1 | Determinates of molecular weight of some selected polymers | ||
| 2 | Know the Preparation and evaluation of solid dispersions,Accelerated stability testing of Aspirin Tablets | ||
| 3 | Know the Stability evaluation of Aspirin at various pH and temperature conditions | ||
| 4 | Know the Preparation and dissolution study of paracetmol tablets and comparison with the marketedproduct | ||
| 5 | Know the Preparation and evaluation of multiple emulsions, Preparation and evaluation of β-cyclodextrin complexes of some drugs | ||
| 6 | Know the solubility and dissolution for few drugs and their respective salts | ||
| 7 | Know the drug release from commercial suspension and emulsion dosage forms | ||
| INDUSTRIAL PHARMACY I-Year II-semester | |||
| Course | Course Code | Course Outcome Number | Course Outcome |
| ADVANCED DRUG DELIVERY SYSTEMS | 6608AV | Upon completion of the course student will be able to | |
| 1 | Know the drugs for CDDS design of the formulation fabrication ofsystems of above drug delivery systems with relevant applications | ||
| 2 | Know the Design, fabrication, evaluation and applications | ||
| 3 | Biochemical and molecular biology approaches to control drug delivery of,Liposomes, Niosomes, Microspheres Nanoparticlese, Resealed erythrocytes |
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| Course | Course Code | Course Outcome Number | Course Outcome |
| PHARMACEUTICAL PRODUCTION TECHNOLOGY | 6608AW | Upon completion of the course student will be able to | |
| 1 | know about the scale up and pilot plant techniques used for all pharmaceutical dosage forms like tablets, capsules, parenterals, aerosols, cosmetics |
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| 2 | Know the neutraceuticals | ||
| 3 | Know the Formulation development of parenteral dosage forms | ||
| 4 | Understand the Aseptic processing operation | ||
| Course | Course Code | Course Outcome Number | Course Outcome |
| NUTRACEUTICALS | 6608AY | Upon completion of the course student will be able to | |
| 1 | The importance of Nutraceuticals in variouscommon problems with the concept of free radicals | ||
| 2 | KnowFood Laws and Regulations | ||
| 3 | Phytochemicals as nutraceuticals | ||
| Course | Course Code | Course Outcome Number | Course Outcome |
| TOTAL QUALITY MANAGEMENT | 6608BB | Upon completion of the course student will be able to | |
| 1 | Know the regulatory guidelines in GMP, GCP, GLP, USFDA, WHO, ISO | ||
| 2 | Acquire vast knowledge regarding the quality control aspects of differentregulatory bodies as per their requirements throughout the world. | ||
| 3 | Gain the knowledge on Good manufacturing practices | ||
| 4 | Know the Globalization of drug industry, present status and scope of pharmaceutical industry in India | ||
| Course | Course Code | Course Outcome Number | Course Outcome |
| DISASTER MANAGEMENT | 6608AM | Upon completion of the course student will be able to | |
| 1 | learn to demonstrate a critical understanding of key concepts in disaster risk reduction and humanitarian response |
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| 2 | critically evaluate disaster risk reduction and humanitarian response policy and practice from multiple perspectives. |
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| 3 | develop an understanding of standards of humanitarian response and practical relevance in specific types of disasters and conflict situations |
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| 4 | critically understand the strengths and weaknesses of disaster management approaches | ||
| 5 | planning and programming in different countries, particularly their home country or the countries they work in |
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| Course | Course Code | Course Outcome Number | Course Outcome |
| ADVANCED DRUG DELIVERY SYSTEMS LAB | 660803 | Upon completion of the course student will be able to | |
| 1 | Know the Study on diffusion of drugs through various polymeric membranes | ||
| 2 | Know the Formulation and evaluation of sustained release oral matrix tablet,oral reservoir system | ||
| 3 | Know the Formulation and evaluation of transdermal films,mucoadhesive system | ||
| 4 | Know the Preparation and evaluation enteric coated pellets / tablets | ||
| Course | Course Code | Course Outcome Number | Course Outcome |
| PHARMACEUTICAL PRODUCTION TECHNOLOGY LAB | 660804 | Upon completion of the course student will be able to | |
| 1 | Know the Preparation of four different types of semisolid forms and evaluation of their performance using in vitro diffusion method |
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| 2 | Know theEvaluation of test sterility for commercial preparations including sterile water for injection and antibiotic injection. |
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| 3 | Know theComparative evaluation of different marketed products (tablets) of the same API | ||
| 4 | Know theDissolution studies of drug in three different bio relevant dissolution media | ||
| 5 | Know theCollecting samples of environment of aseptic room and counting the colonies | ||
| 6 | Know theValidation of one-unit operation (eg. Mixing) and development of protocol | ||
| M. Pharmacy II Year I- SEMESTER INDUSTRIAL PHARMACY | |||
| Course | Course Code | Course Outcome Number | Course Outcome |
| SCALE UP AND TECHNOLOGY TRANSFER | 6603BB | Upon completion of the course student will be able to | |
| 1 | Understand Manage the scale up process in pharmaceutical industry. | ||
| 2 | Gain the knowledge on Assist in technology transfer. | ||
| 3 | To establish safety guidelines, which prevent industrial hazards | ||
| M. Pharmacy II year II-Semester ( PCI Regulation) | |||
| Course | Course Code | Course Outcome Number | Course Outcome |
| RESEARCH WORK | Upon completion of the course student will be able to | ||
| 1 | Perform the work in the innovative and systematic way | ||
| 2 | Assemble the information into a more realistic draft ethically and conclude the contents. | ||
| 3 | Prepare the thesis by arranging the contents in a orderly manner and preparation of the research manuscript. | ||
| Course | Course Code | Course Outcome Number | Course Outcome |
| DISCUSSION/FINAL PRESENTATION | Upon completion of the course student will be able to | ||
| 1 | Prepare the presentation based on the results obtained in the research work | ||
| 2 | Explain outcome of their project along with further scope for research. This develops their oratory and leadership skills | ||