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PROGYMS Pharmaceutical practices Total Quality Management (TQM) that meets GMP standards over the whole production process. Quality Control and Risk Assessment at each link forms a complete stringent quality control system as the following:

  • Product Specification (with comprehensive formulation and packaging details)
  • Quality Analysis (Heavy Metals, FTIR, AAS and HPLC)
  • Process Validation
  • Test Method Development
  • Observatory Period (14 Days Quality Inspection per batch)
  • Release for Supply
  • Stability Test (Microbial, Physical, Sensory, Shelf Life Test)

Workshop And Quality Control System Up To GMP Standards

  • Quality Control over the entire process from raw materials to finished products
  • Whole-course traceable records
  • Supplier Audit Program (UL-VS, BSCI)
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