What Are Cloud Services and How to Validate Them
Borislav Milev is a CSV expert. In this podcast episode, he explains what cloud computing is and how to validate it in a GMP environment.
Pharma Trends: The Return of the FDA Warning Letters [Simone Ammons] Simone (George) Ammons
How to Qualify Your Equipment 101 Vlatko Kantardjioski
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)
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Learn More Here
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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Tagged as: Qualification, Equipment Qualification, GMP.
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.
Borislav Milev November 23, 2020
Borislav Milev is a CSV expert. In this podcast episode, he explains what cloud computing is and how to validate it in a GMP environment.
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