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How to Qualify Your Equipment 101

Vlatko Kantardjioski December 7, 2020 531

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In this podcast episode, Vlatko Kantardjioski gives an amazing overview of equipment qualification in the pharmaceutical industry.

Vlatko is a Quality Assurance Specialist and served in leading positions in various equipment qualification projects.

By listening to or watching this episode, you will learn about:

– User Requirement Specifications
– Design Qualification (DQ)
– Factory Acceptance Test (FAT)
– SAT (Site Acceptance Test)
– Installation Qualification (IQ)
– Operational Qualification (OQ)
– Performance Qualification (PQ)


Master Class: Managing Deviations From A to Z

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We start on January 18, 2021.
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Information on good manufacturing practices (GMP) in the life science industry is scattered, vague and poorly organized. We have chosen to solve this problem by organizing the best possible GMP webinars and courses to ensure we deliver all the information you need in a concise, engaging and clear format. All events are free and open to anyone in the industry.

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Vlatko Kantardjioski

Vlatko is a GMP professional with operational and project hands-on experience throughout various pharmaceutical industry areas: manufacturing, product and process development, technology transfer, CMO and regulatory audits, equipment qualification, validations, and quality assurance.

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