ISACA is a key collaborator in the Case for Quality collaborative community's Voluntary Improvement Program (VIP) alongside the MDIC, FDA CDRH and medical device industry. VIP helps device makers design, build and deliver safer products to patients faster by identifying process inefficiencies and implementing best practices that accelerate medical device improvements.As an incentive, participants benefit from several FDA regulatory opportunities to help speed improvements to device quality and manufacturing by means of modified inspection planning and bundled PMA and Site Change submissions with reduced review timeframes. These regulatory opportunities are detailed in the FDA Guidance “Fostering Medical Device Improvement: FDA Activities and Engagement with the Voluntary Improvement Program.”Voluntary Improvement Program participant outcomes include increased speed to market, improved production capacity, reduced regulatory burden, better employee morale & more! Visit the ISACA booth to learn how to accelerate a quality culture in your organization.