Post Graduate Programme in Quality Control and Assurance Syllabus 2025: Subjects, Specializations, and Semester-wise Syllabus

  • course years 1 Years
  • type of course Post Graduate
  • course stream Science
  • course type Full Time
Written By universitykart team | Last Updated date Oct, 09, 2024

The program's syllabus is designed to provide students with in-depth knowledge and practical skills related to quality control and assurance. Courses cover a wide range of topics, including quality management principles, statistical quality control, regulatory compliance, quality auditing

Syllabus for PGP in Quality Control and Assurance Course

The Post Graduate Programme in Quality Control and Assurance typically encompasses a comprehensive syllabus that focuses on the principles, methodologies, and best practices related to quality control and assurance in various industries. Core subjects often include quality management systems such as ISO standards, statistical quality analysis, process improvement methodologies, and regulatory compliance. Students delve into topics such as quality audits, risk management, and supply chain quality management. Advanced coursework may explore areas like Lean Six Sigma, total quality management (TQM), and advanced statistical techniques for quality assurance. Practical components often involve hands-on quality assessment projects, case studies, and the application of statistical tools and software for quality analysis. Graduates of this program are equipped with the knowledge and skills required to manage and lead quality assurance programs, ensure compliance with industry standards, and drive continuous improvement in product and service quality. Specific topics and course offerings may vary among institutions offering the program.

Syllabus of Post Graduate Programme in Quality Control and Assurance

S.NoSubjects
 1Quality Control vs. Quality Assurance                                               
2Good Laboratory Documentation
3Quality Systems/Quality Assurance
4Method Development and Validation
5ASTM Methods
6Working in a cGMP Environment
7Process Control
8Process Deviations and Investigations
9CAPA systems
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