Sterile Filtration Skid (LVP) – Qualification Certificate Template

Qualification Certificate

Equipment: Sterile Filtration Skid (LVP)

Subcategory: IV Infusions (LVP/SVP – Bags/Bottles)

Area: Production

DQ/IQ/OQ/PQ Flags: Yes / Yes / Yes / Yes

Requalification Frequency: 12 Months

Equipment Identifiers

Equipment ID: [Equipment ID Placeholder]

Serial Number: [Serial Number Placeholder]

Protocol References

DQ Protocol: [DQ Protocol Reference Placeholder]

IQ Protocol: [IQ Protocol Reference Placeholder]

OQ Protocol: [OQ Protocol Reference Placeholder]

PQ Protocol: [PQ Protocol Reference Placeholder]

Execution Dates

DQ Execution Date: [DQ Execution Date Placeholder]

IQ Execution Date: [IQ Execution Date Placeholder]

OQ Execution Date: [OQ Execution Date Placeholder]

PQ Execution Date: [PQ Execution Date Placeholder]

Calibration Status

Calibration Status: [Calibration Status Placeholder]

Deviations Summary

Deviations Summary: [Deviations Summary Line Placeholder]

Overall Qualification Statement

The Sterile Filtration Skid (LVP) has been successfully qualified according to the established protocols and meets all operational requirements.

Approvals

Approved By: [Approver Name Placeholder]

Date of Approval: [Date of Approval Placeholder]

Next Due Date

Next Due Date: [Next Due Date Placeholder]

See also  Fluid Bed Dryer (FBD) – Validation Summary Report (VSR) Template