Validation of Computerized Systems and Equipment ensures that a computerized system or equipment is appropriate for its intended use. A typical validation life cycle consists of the following phases: IQ, OQ and PQ.
Computerized Systems or Software that perform GxP related functions in the Life Science industry must be qualified or validated.
Computerized Systems may include networks (wired and wireless), workstations, operating system & application software, instrument software,
equipment automation software, and any interfaces to other GxP systems.
Pharmaceutical Services Corporation offers a complete range of services for your computer validation needs.
Our computerized systems and software validation services include but are not limited to:
- Process Control Systems (PCS)
- Building Management Systems (BMS)
- Laboratory Information Management Systems (LIMS)
- Electronic Document Management Systems (EDMS)
- Product Software
If you have a need for Computer Software Implementation and Validation, please
Contact Us.