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Since these concepts are complex, it’s best to understand them one by one. IQ, OQ, PQ protocols are methods for demonstrating that equipment being used or installed will offer a high degree of quality assurance such that production processes will consistently manufacture products that meet quality requirements. Preparing for a Life Science Validation Project Inside, you’ll find seven essentials to building an efficient and effective validation team along with expert insights from staffing professionals who routinely help life science organizations build successful project teams. If you’re planning a validation project, be sure to grab our free guide. This guide offers a clear and simple explanation of what these concepts are, why they’re important, what makes them successful, and a model for connecting with professionals who can plan and execute these types of projects. One of the key sets of protocols within equipment validation is Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). In the highly-regulated pharmaceutical, medical devices, and clinical industries, even tiny inconsistencies can compound into serious issues without the proper qualification and validation protocols in place.Īs a component of quality assurance, equipment validation is absolutely critical to producing consistent, high-quality products.

Soundcraftsmen phase control regulation pcr 800