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Last Updated: October 1, 2026
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In this session we will explore the This is an excerpt from the course " In this video, Helena Hjälmefjord, This time we will be discussing In this webinar we will simplify the approach to validating software for QMS and Equipment to ISO 13485, Clauses 4.1.6 and 7.5.6. Learn AMV and its key parameters in pharmaceutical quality control with practical examples. Annex 3 Guidelines on good manufacturing practices: validation, Appendix 7: non‑sterile
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