Lectures

Medical Device Hazard Analysis Following ISO 14971 - 2017

When: Wed., Nov. 8, 12-1 p.m. 2017

Overview: The US FDA expects that as part of a product development Design Control Program risk management will be conducted. FDA recommends using ISO 14971 as a guide and has accepted it as a recognized standard. Why should you Attend: FDA expects that as part of a product development program risk management will be conducted. FDA recommends using ISO 14971 as a guide and has accepted it as a recognized standard.

Price: $ 150.00

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