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.
- Design Qualification for FFS Machine
- Installation Qualification for FFS Machine
- Performance Qualification Protocol for FFS Machine
- Performance Qualification Report for FFS Machine
- Design Qualification for Garment Cabinet
- Installation Qualification for Garment Cabinet
- Operational Qualification of Garment Cabinet
- Performance Qualification Protocol for Dynamic Garment Cabinet
- Performance Qualification Report for Dynamic Garment Cabinet
- Design Qualification for Leak test apparatus
- Design Qualification for S S Jacketed Manufacturing Vessel
- Installation Qualification for SS Jacketed Manufacturing Vessel (2000 Liter)
- Operational Qualification for SS Jacketed Manufacturing Vessel (2000 Liter)
- Performance Qualification Protocol for SS Jacketed Manufacturing Vessel (2000 Liter)
- Performance Qualification Report for SS Jacketed Manufacturing Vessel (2000 Liter)
- Design Qualification for Sticker Labeling Machine
- Installation Qualification for Garment Washing Machine
- Installation Qualification for Sticker Labeling Machine
- Operational Qualification for CIP SIP Module (500 Litre)
- Operational Qualification for Dynamic Pass Box
- Operational Qualification for Garment Washing Machine
- Operational Qualification for Sticker Labeling Machine
- Operational Qualification for Vacuum Leak Tester
- Operational Qualification for Vertical Autoclave
- Performance Qualification Protocol for Vertical Laminar Air Flow
- Performance Qualification Protocol for Vertical Autoclave
- Performance Qualification Protocol for Vacuum Leak Tester
- Performance Qualification Protocol for Sticker Labeling Machine
- Performance Qualification Protocol for Garment Washing Machine
- Performance Qualification Protocol for CIP SIP
- Performance Qualification Protocol for Dynamic Pass Box
- Performance Qualification Report for Vacuum Leak Tester
- Performance Qualification Report for Vacuum Leak Tester
- Performance Qualification Report for Vertical Laminar Air Flow
- Performance Qualification Report for Sticker Labeling Machine
- Performance Qualification Report for CIP-SIP Module
- Performance Qualification Report for Vertical Autoclave
- Performance Qualification Protocol for CIP SIP Module (500 Ltr)
- Performance Qualification Report for CIP-SIP Module (500 Litre)