MasterControl
GxP Lifeline Newsletter
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June | 2022
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EU MDR vs. U.S. QSR and the Role of Digitization
See why there are more similarities than differences in how medical devices are regulated in the U.S. and Europe.
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Bringing ISO 13485 to 21 CFR Part 820
Learn how the FDA’s proposed changes would make it easier to be FDA compliant and ISO certified.
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How Modern EQMS Solutions Are Powering Pharma’s Digital Revolution
Pharma leaders are using innovative EQMS tools to overcome today’s big challenges – are you keeping pace?
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The CAPA Magnificent Seven
A closer look at a classic film can teach you seven ways to simplify your corrective action/preventive action process.
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…And Check Out This Month’s Most Popular Blog Post
7 Key Concepts in the FDA’s Quality System Guidance for Pharma
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