Quality Management System

Quality Management System


Pharmatec Quality Operation System is based on DRAP, WHO and EU GMP guidelines which help to ensure the high quality of pharmaceutical products which is expected by the customers as well as to implement the quality objectives of the company comprehensively in all the company departments. The skilled senior management is responsible for the implementation of the system and its upgradation.


A well-defined system for the assurance of quality is strictly implemented in Pharmatec. All controlled documents regarding quality management system are generated in the light of DRAP, WHO and EU GMP guidelines. There is a comprehensive arrangement for the management and assurance of the quality which includes but not limited to:
  • IPC Checks
  • Document Control
  • Vendor Qualification
  • Deviation Management
  • Change Control management
  • CAPA Management
  • Risk Assessment
  • Validation & Qualification

Quality Assurance framework in Pharmatec is designed to instill confidence among stakeholders as well as customers.


The Quality Control laboratory in Pharmatec is highly equipped and is managed by a team of highly skilled chemists, microbiologists and pharmacists which plays a very active and competent role in Validation and Batch release activities. Our QC laboratory is well equipped to handle all the different dosage forms.