Training Needs Analysis (TNA)
Industry Center for Excellence Programs for Undergraduates (ICOE)
Good Manufacturing Practices (GMP)
Quality, Safety & Environment
Productivity & Quality Improvement Programs
Human Capital Development

Good manufacturing practice (GMP) guidelines by World Health Organization (WHO) provide guidance for manufacturing, testing, and quality assurance in order to ensure that a drug or food product is safe for human consumption and meets regulatory product registration requirements. Many countries have legislated that food, pharmaceutical and medical device manufacturers follow GMP procedures and create their own GMP guidelines that correspond with their legislation.

The GMP guidelines covers aspects of manufacturing process, documentation & record keeping, people management, training, internal auditing, continuous improvement and complaints management. The Good Laboratory Practice or GLP concept covers laboratory Quality management system for reliable and valid testing & reporting of results that is a vital component of GMP.

Programs offered under GMS Series are as below:

  • Module 1- Quality Management System (QMS) and Laboratory Quality Management Systems (ISO/IEC 17025:2005)
  • Module 2- Good Quality Control Laboratory Practices (GLP)
  • Module 3- Microbiological Industrial Best Practices (NEW!!)
  • Module 4- Effective and Competent Certified Internal Quality Auditor
  • Module 5- Effective Problem Solving and Root Cause Analysis for Quality and Productivity Improvement
  • Module 6: Materials Management & Supply Chain (NEW!!)
  • Module 7: International GMP standard for Manufacturing Infrastructure: Facilities, Utilities & Equipment (NEW!!)

[References: Publications by American Society for Quality (ASQ) and International Society for Pharmaceutical Engineering (ISPE)]


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