EQUIPMENT VALIDATION / QUALIFICATION (IQ,OP & PQ)
● A system needs to be fully qualified to produce high-quality products in a consistent manner. Therefore Equipment Validation is of utmost importance. Equipment Validation comprises a series of system qualifications, such as Design, Installation, Operational, and Performance Qualification, that provide a high degree of assurance of the consistent, expected functioning of equipment.
● This webinar on equipment validation in the pharmaceutical industry focuses on Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) or Continuous Qualification (CQ), Qualification Protocol Test Case Examples, Power off / Power failure tests, Door Open tests, Alarm testing, Loaded and Empty Mappings, Instrument/equipment calibration.
● Aspirants who want to become Equipment Validation Specialist, Validation Engineer or Specialist, Process Engineer or Project Engineer, Quality Assurance Specialist, Quality Control Specialist, Maintenance Engineer, Maintenance Technician, Senior Validation Manager should attend this webinar on equipment validation in the pharmaceutical industry.
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