FDA Discusses Driving a Culture of Change for Devicemakers Webinar

Industry experts and regulators discuss the need to shift the focus from compliance to quality by giving greater focus and emphasis to critical-to-quality practices throughout the lifecycle in the Medical Device Industry.
Hear their perspective on the Case for Quality (CfQ) Initiative and the effect that CfQ will have on med-tech manufacturers, healthcare providers, regulators and ultimately the patient.  A panel discussion and Q&A is part of this webinar . . .

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