Ft Myers, FL. Support development creation of regulatory documents in accordance with MDD, MDR ISO 13485:2016, FDA 21 CFR Part 820, MDSAP for medical device manufacturing company; conduct regulatory literature reviews for medical devices; develop write procedures and...
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Ft Myers, FL. Support development creation of regulatory documents in accordance with MDD, MDR ISO 13485:2016, FDA 21 CFR Part 820,...
Read More