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M.Pharm ( Pharmaceutical Analysis)

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M.Pharm ( Pharmaceutical Analysis)

   Department of Pharmacy

Programme Level

Post Graduate

Duration

2 Years

About the Programme

The M.Pharm Pharmaceutical Analysis programme focuses on the study and application of techniques used to identify, quantify, and ensure the quality and purity of pharmaceutical substances. It involves both theoretical and practical training in various analytical methods such as spectroscopy, chromatography, thermal analysis and titrimetry. This programme equips students with the skills necessary to perform critical quality control and assurance tasks in pharmaceutical industries, research laboratories, and regulatory agencies. It plays a vital role in ensuring drug safety, efficacy, and compliance with international standards.

Eligibility

B.Pharm with minimum 55% marks

Fee Structure

Duration
2 Years
Tuition Fee (per annum)
90.000
Exam Fee (per annum)
20,000

Program Structure

Program Structure

Programme Outcomes

01

Analyze and interpret experimental data in the development of analytical methods for bulk pharmaceuticals and pharmaceutical dosage forms.


02

In his or her academic and professional life, develop a problem-based learning strategy and analytical thinking.


03

Use critical thinking abilities to do research, including investigation, application, analysis, innovation, and evaluation of information, data, and documents.


04

Develop scientific communication and research writing skills.


05

Use the knowledge and abilities acquired in University to obtain respect in the professional and social circles.


06

Conduct multidisciplinary research in collaboration with other healthcare communities to develop novel solutions.


07

Take a part in healthcare activities to raise public knowledge regarding the proper and safe use of medications.


08

Demonstrate environmentally sustainable products and procedures in order to protect public health.


09

In both personal and professional efforts, perform ethical behaviors and moral principles.


10

Approach professional problems with a mind-set of lifelong learning.


Programme Educational Objectives

01

Enable graduates to apply regulatory guidelines and quality standards (such as ICH, USP and WHO) in the evaluation, validation and documentation of pharmaceutical products.


02

Achieve successful careers in industry, academia, research and regulatory sectors by fostering critical thinking, ethical practices and lifelong learning.


03

Encourage innovation and research in the field of pharmaceutical analysis, including method development, stability studies, and advanced analytical instrumentation.


Programme Specific Outcomes (PSOs)

01

Apply advanced knowledge and techniques in pharmaceutical analysis to ensure the identity, purity, quality, and quantity of drug substances and formulations using modern instrumentation and regulatory guidelines.


02

Demonstrate proficiency in the interpretation and implementation of national and international pharmacopeial standards, regulatory requirements (e.g., ICH, FDA, WHO), and Good Laboratory Practices (GLP) in analytical laboratories.


03

Examine critique, organize, improvise, and manage documents, data, and information pertaining to the Pharmaceutical manufacturing, Quality Control and Quality Assurance.