Best Practices for Medical Device Reporting (MDR), Recall, Reports of Corrections and Removals

This webinar will discuss requirements and compliance under the applicable FDA regulations for medical device reporting (MDR), recall and reports of corrections and removals in the US. It is designed to help the audience develop, maintain and implement adequate procedures.

20 de agosto de 2015 | Palo Alto (Estados Unidos)

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Online Event

2600 E. Bayshore Road

Palo Alto (Estados Unidos)

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ComplianceOnline

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