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Your Ultimate Guide to 21 CFR Part 11 | Electronic Records & Signatures | US FDA GxP Requirements
Автор: Clinical Research x360
Загружено: 15 апр. 2025 г.
Просмотров: 123 просмотра
Описание:
In this podcast we explain in detail the US FDA 21 CFR Part 11 Guideline that is widely used in pharmaceutical, biotechnology, or clinical research fields. This guideline is crucial to maintain the integrity of electronic records and signatures. IN this session we break down 21 CFR Part 11, that sets the standards for electronic records and signatures in regulated industries. which helps in maintaining data integrity and ensuring compliance with regulatory requirements.
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