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 . . .
You've reached premium content. Please email email@example.com for a complementary access code to view this premium content.