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Form Fill Seal Equipments qualifications in Pharma are crucial. To prepare sterile items, form fill seal (FFS) technology uses automated computer control. A producer needs up-to-date, dependable packaging equipment in order to make better packages more rapidly and profitably. Form-fill-seal technology is constantly evolving. Reduced contamination during production in a confined, sterile chamber of a machine is the goal of form-fill-seal technology. Therefore, there shouldn’t be any human intervention during the production of sterile products to lessen the possibility of contamination. It can be used for IV infusion bottles in the pharmaceutical business. All phases in this procedure, including the creation of the container, filling it with content, and sealing it, are carried out automatically, sequentially, and in a closed sterile chamber of the machine. The rate of product contamination is decreased by this method. With a high assurance of sterility, it boosts output rate at a very cheap operational cost.

  1. Design Qualification for FFS Machine
  2. Installation Qualification for FFS Machine
  3. Performance Qualification Protocol for FFS Machine
  4. Performance Qualification Report for FFS Machine
  5. Design Qualification for Garment Cabinet
  6. Installation Qualification for Garment Cabinet
  7. Operational Qualification of Garment Cabinet
  8. Performance Qualification Protocol for Dynamic Garment Cabinet
  9. Performance Qualification Report for Dynamic Garment Cabinet
  10. Design Qualification for Leak test apparatus
  11. Design Qualification for S S Jacketed Manufacturing Vessel
  12. Installation Qualification for SS Jacketed Manufacturing Vessel (2000 Liter)
  13. Operational Qualification for SS Jacketed Manufacturing Vessel (2000 Liter)
  14. Performance Qualification Protocol for SS Jacketed Manufacturing Vessel (2000 Liter)
  15. Performance Qualification Report for SS Jacketed Manufacturing Vessel (2000 Liter)
  16. Design Qualification for Sticker Labeling Machine
  17. Installation Qualification for Garment Washing Machine
  18. Installation Qualification for Sticker Labeling Machine
  19. Operational Qualification for CIP SIP Module (500 Litre)
  20. Operational Qualification for Dynamic Pass Box
  21. Operational Qualification for Garment Washing Machine
  22. Operational Qualification for Sticker Labeling Machine
  23. Operational Qualification for Vacuum Leak Tester
  24. Operational Qualification for Vertical Autoclave
  25. Performance Qualification Protocol for Vertical Laminar Air Flow
  26. Performance Qualification Protocol for Vertical Autoclave
  27. Performance Qualification Protocol for Vacuum Leak Tester
  28. Performance Qualification Protocol for Sticker Labeling Machine
  29. Performance Qualification Protocol for Garment Washing Machine
  30. Performance Qualification Protocol for CIP SIP
  31. Performance Qualification Protocol for Dynamic Pass Box
  32. Performance Qualification Report for Vacuum Leak Tester
  33. Performance Qualification Report for Vacuum Leak Tester
  34. Performance Qualification Report for Vertical Laminar Air Flow
  35. Performance Qualification Report for Sticker Labeling Machine
  36. Performance Qualification Report for CIP-SIP Module
  37. Performance Qualification Report for Vertical Autoclave
  38. Performance Qualification Protocol for CIP SIP Module (500 Ltr)
  39. Performance Qualification Report for CIP-SIP Module (500 Litre)

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