Empower your employees and reduce regulatory burden – discover the power of VIP
Learn more now about the Voluntary Improvement Program (VIP), delivered by ISACA in collaboration with US FDA and MDIC.
Discover how VIP uses a globally accepted maturity model combined with FDA regulatory opportunities to provide medical device manufacturers with a clear view of their business capabilities, identifying gaps and allowing for continuous improvement.
Download the VIP Playbook to explore how VIP:
- Improves synergies between product development and product manufacturing
- Drives continuous process improvements while strengthening quality culture
- Identifies manufacturing facility issues
- Supports the evolving advancement of product quality
- Builds a strong relationship with US FDA

