Installation Qualification (IQ) is a crucial step in the validation process in the pharmaceutical sector.
IQ refers to the documented verification that all aspects of system installation comply with predefined specifications. This process typically includes the inspection of installations, equipment, instruments, and other components.
The primary goal of IQ is to ensure that the installation has been carried out correctly and that the system functions properly. A successful IQ is essential as it forms the foundation for further validation activities, such as Operational Qualification (OQ) and Performance Qualification (PQ).