The Voluntary Improvement Program (VIP) helps device makers design, build and deliver safer products to patients, faster. As part of the FDA’s case for quality initiative, this program identifies process inefficiencies and helps device makers implement best practices that accelerate medical device improvements. Participant outcomes include increased speed to market, improved production capacity, reduced regulatory burden & more.
Read details in the FDA Guidance “Fostering Medical Device Improvement: FDA Activities and Engagement with the Voluntary Improvement Program” released on 14 September 2023.