Managing quality through the supply chain with UDI
Be prepared for UDI requirements with USDM’s implementation and compliance solutions and expert guidance on global regulations. USDM Life Sciences is the industry leader in Unique Device Identification (UDI) regulatory compliance solutions for the medical device industry. We have well-established relationships with the most prominent IT vendors in the world, and an experienced team of subject matter experts led by Jay Crowley
, who developed the framework and authored key requirements for the FDA’s UDI system. We can help your organization execute a program to support your UDI efforts.
Tailored to the UDI Final Rule in the United States and the UDI Regulation in the European Union (EU), our UDI guidance and implementation solutions can help you utilize the benefits of UDI while achieving regulatory compliance.
We offer our customers the following UDI guidance and services.
Global Readiness Services
- UDI Audits
- UDI Program Design and Execution
- UDI Product Analysis (class III, FDASIA, II, I)
- UDI Business Process Analysis and Improvement
- UDI Policy Development
- UDI Regulatory Guidance
Global Regulatory Database Submission Services and Support
- Submission Strategy
- Submission Preparation
- Submission Support
- UDI System Enhancements and Validation
UDI Education and Training
- UDI Regulation Overview (e.g., US FDA UDI Final Rule, MDR/IVDR)
- UDI Regulatory Database* Training
Still Have UDI MDR Questions?
View extra materials:
Webinar: Evolving Global UDI Product Data Requirements
Blog: More Medical Device Implications of Brexit
Webinar: How to Comply with Saudi Arabia UDI Requirements
Blog: Key differences in the requirements for SFDA UDI and US & EU UDI
Podcast: EP 3: Global UDI and EU MDR Requirements