Utilising DMAIC for Regulatory Decision Cycle Time Optimisation
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Utilising DMAIC for Regulatory Decision Cycle Time Optimisation
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According to FDA guidelines for medical device manufacturers, decision making for reportability purposes to regulatory authorities is required within 30 days of a potential complaint reception. In this podcast, Sebastian Fishman, Project Coordinator at Allergan Medical, joins us to explore how to speed up this cycle time and eliminate errors.
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