M.PHARM (PHARMACEUTICALANALYSIS)
PO1: To deal with various advanced instrumental techniques for separation, identification, characterization, and quantification of drugs in bulk, formulation & biological samples.
PO2: To know the science of detection of impurities, stability of the product and regulatory guidelines.
PO3: To impart knowledge on analysis of food constituents and finished food products, food additives, the pesticides and the regulations of food and legislations of food products
PO4: To understand validation and its application in industry, their methodologies and application in manufacturing processes
PO5: To know about quality assurance aspects of pharmaceutical industries such as CGMP, Documentations, certifications, GLP, and other regulatory affairs
PO6: To create a talent pool by involving students in research projects and to make students undertake research projects under faculty guidance for publication
M.PHARM (PHARMACEUTICAL QUALITY ASSURANCE)
PO 1: Develop consistency in quality related problem identification, analysis and solving.
PO 2: Conceptualise research ideas, develop oral and written communication skills including soft skills, frame and evaluate hypothesis by collating and interpreting data to draw meaningful conclusions.
PO 3: Inculcate a sense of fair play, social values and professional ethics.
PO 4: Acquire skills in managing human, financial and other resources efficiently to achieve the project objectives and stakeholder’s satisfaction.
PO 5: Demonstrate competency in designing and using various quality tools for troubleshooting.
PO 6: Acquire skills in implementing modern tools like Quality by Design (QbD), Process Analytical Technology (PAT), Design of Experiments (DoE) and Technology Transfer etc.
PO 7: Demonstrate competency in the area of pharmaceutical quality systems, drug development research and drug regulations.
M.PHARM (PHARMACOLOGY)
PO 1: Acquire a strong knowledge in theoretical & Practical aspects of Pharmacology subjects along with necessary skills.
PO 2: Gain Knowledge on modern Pharmacological tools and software’s associated with Research and development.
PO 3: Must be able to compete in the modern Pharmacological domains of the industry like Pharmacovigilence, Regulatory affairs and new drug developments.
PO 4: Able to apply knowledge on new natural, synthetic and semi synthetic drug developments and must be able to provide most modern data acquisition and analysis system in the biological and Pharmacological research.
PO 5: Demonstrate High throughput screening mechanism in new drug discovery and development of challenging and expensive activities of the Pharmaceutical Industry.
PO 6: Succeed in pharmaceutical industry or academics through innovative teaching methodologies that stimulates students to self-learning and extend their knowledge.
M.PHARM (PHARMACEUTICS)
PO 1: Impart knowledge on the novel drug delivery systems, approaches, criteria for the selection of polymers and drugs and their formulation and evaluation.
PO2: To know various preformulating elements, industrial management and GMP considerations, Pilot Plant Scale up Techniques, Stability testing, sterilization and packaging of dosage forms.
PO3: To impart knowledge and skills for dose calculations, dose adjustments and apply biopharmaceutics theories in practical problem-solving. The pharmacokinetic models, bioequivalence and potential clinical pharmacokinetic problem analysis
PO4: Skill development in Pharmaceutical research, Pharmacoinformatic, in drug development in Computational modelling, Preclinical development, clinical development, Artificial Intelligence and Robotics, and Computational fluid dynamics.
PO5: To impart knowledge and skills necessary for cosmetics and cosmeceuticals, their safety and efficacy and current technologies in cosmetic industry.
PO 6: To create a talent pool by involving students in research projects and to make students undertake research projects under faculty guidance for publication.
PO7: To foster ambitious desire among students to undertake higher studies and career growth.
PO 8: Apply knowledge to create newer technology and skills in pharmaceutical technology development and research.
M.PHARM (PHARMACEUTICAL REGULATORYAFFAIRS)
PO1: Possess knowledge, comprehension of the core and basic knowledge
associated with the profession of Pharmaceutical Regulatory Sciences, including
drug development process, dossier preparation, good manufacturing practices,
clinical trials and human research.
PO2: Demonstrate effective planning abilities and elements that are
necessary to accumulate the regulatory submissions including time management,
resource management, delegation skills and organizational skills. Develop and
implement plans and organize work to meet deadlines.
PO3: Utilize the principles of scientific enquiry, thinking
analytically, clearly and critically, while solving problems and making
decisions during daily practice. Find, analyze, evaluate and apply information
systematically. and shall make defensible decisions while reviewing and
submission of dossiers to regulatory markets.
PO4: Learn, select, and apply appropriate methods and procedures,
resources and modern regulatory-related computing tools with an understanding
of their limitations.
PO5: Collaboration and Team Work: Understand and consider the human
reaction to change, motivation, issues, leadership and team-building when
planning changes required for fulfilment of practice, professional and societal
responsibilities which also includes interpersonal skills, knowledge sharing
and strategy in between members of a virtual team.
PO6: Use ethical frameworks, apply ethical principles while making
decisions and take responsibility for the outcomes associated with the
decisions in clinical research and clinical investigations.
PO7: Understand, analyze and communicate the value of their professional
roles in society and business development and be reliable with critical
thinking and regulatory writing skills.
PO8: Appreciation of and ability to learn from and work with people from
diverse linguistic and cultural backgrounds. It should emphasize how regulatory
strategy increases a products chance of entering a market and staying there.
Once cross-functional teams understand regulatory strategy and its importance
in product development and inter-team communication.
PO9: Individual's ability to turn ideas into practice. Like finding new
opportunities to share information and concepts. Generating options and
solutions to cope with changes. It involves imagination, novelty and
risk-taking, as well as the ability to plan and manage projects.
PO10: Function of knowledge, curiosity, imagination, and evaluation. The
greater individual knowledge base and level of curiosity, the more ideas,
patterns, and combinations will achieve, which then correlates to creating new
and innovative products and services.
PO11: Recognize the need for, and have the preparation and ability to
engage in independent and life-long learning in the broadest context of
technological change.