Post Market Surveillance & Adverse Event Reporting What is an
Post Market Surveillance & Adverse Event Reporting What is an
Post Market Surveillance & Adverse Event Reporting What is an
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Life cycle of medical devices & Principal StakeholdersD<strong>is</strong>posalDEVUseRefurb.M,RA/CAB,HSUseMFGM & S- RA / CAB authorizesmarketing- M<strong>an</strong>ufacturer puts onmarket- Healthcare System gr<strong>an</strong>tsreimbursement or not
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