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:
Listing Documentation
Raw Material Inspection (Zero Tolerance Policy, only 100% PURE ingredients selected)
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)