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Design Control for Medical Device Professionalsin Berlin from 10.09.2012 - 11.09.2012
This continually updated course covers current FDA regulatory compliance with respect to developing medical devices. A focus is placed on basic regulation and the FDA’s supplemental guidelines. Among the topics to be discussed are: the context of design control within the overall quality system and regulation, design control procedures, forms, records, safety/risk management strategies, documentation strategies, manufacturing transfer strategies, and strategies for integrating general quality system procedures into design control.
|Event Date:||10.09.2012 to 11.09.2012|
The Berlin Hilton
Center for Professional Innovation & Education (CfPIE)
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