This video is about Installation Qualification of pharmaceutical equipment| IQ of pharmaceutical equipment
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Installation Qualification of pharmaceutical equipment| IQ of pharmaceutical equipment
Systems and equipment should be correctly installed in accordance with an installation plan and installation qualification protocol.
Installation qualification should include identification and verification of all system elements, parts, services, controls, gauges, instruments and other components.
There should be documented records for the installation (installation qualification report) to indicate the satisfactoriness of the installation, which should include the details of the supplier and manufacturer, system or equipment name, model and serial number, date of installation, spare parts, relevant procedures and certificates.
Installation Qualification includes following verifications (but not limited to)
Documents Verification
Drawings verification
Major components verification
MOC verification of components.
Identification of instruments requiring calibration.
SOP for operation, cleaning and maintenance identification
Utilities requirement verification
Requirements which need to be verified against URS / RA
Environmental Health and safety parameters verification.
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