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How To Validate Your Computerized Systems

Daniel Milek October 26, 2020 429

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Computer system validation (CSV) is more crucial now than ever. The reason for that is the digital transformation that pharma companies undergo in recent years. Additionally, equipment and software become obsolete with time. Therefore, you need to replace it or update the software and validate it according to the current GMP standards.

In this podcast episode, Daniel Milek, a CSV expert from Data Integral Ltd, provides precious guidance on how you should go about your system validations.

Here are some of the topics you will learn about, listening to or watching this podcast episode:

💡 The Stages of a Successful CSV
💡 How Is CSV Different From Other Process Validations
💡 How to Train People in CSV
💡 How to Use Screenshots Right for CSV
💡 The Biggest Misconceptions With Computer Systems

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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.

Browse Upcoming Free GMP Webinars


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Daniel Milek

Daniel is the founder of Data Integral. He is an expert in providing Data Integrity, Data Governance, CSV, and Project Management solutions for companies engaged in the manufacture and testing of licensed medicinal products.

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