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QMS ref

توسط Chandrasekaran M. 5,218 KB • 25 فایل

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3_choosing_performance_indicators_day_one.pdf
21cfr&iso13485.pdf
9001 13485 mdr mdd.doc
ASQ13485[1].ppt
audit checklist - (iso 13485 and mdd).doc
Backup of SG3_%20ISO%2013485_2000,%20An%20Overview.pdf
blank ISO 13485-9001-21cfr820 Checklist.doc
Canadaregs2006.pdf
CMDCAS ISO 13485 Audit - gd210-eng.pdf
dec of conformity.doc
how to complete the application form for a new device licence.pdf
interdependent medical devices.pdf
iso 13485 documentation requirements.doc
labeling mdd regs.pdf
MEDICAL DEVICE ACT (Act 737)_2012.pdf
MHLW #169 vs ISO 13485 2003.xls
Required Quality Records for ISO 13485.doc
Supplier Audit Questionnaire example.pdf
supplier qualification of a medicines manufacturer.pdf
Supplier Qualification Quidelines example.pdf
Supplier Quality System Audit Checklist example.pdf
Understanding_ISO13485-practical guide.pdf
What_Is_ISO_13485-practical guide.pdf
What_Is_ISO_13485.pdf

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