Ensure Compliance, Enhance Quality
In today’s regulatory landscape, managing and tracking quality data across departments is no longer optional—it’s critical. Teamcenter Data Traceability, a core offering of Siemens’ Closed Loop Quality and Compliance (CLQC) solution, provides a connected digital backbone to trace, manage, and ensure quality across the medical device lifecycle.
Whether it’s product design, manufacturing records, change control, or post-market data—Teamcenter empowers teams to stay compliant, collaborate efficiently, and reduce risks.
Unlike traditional paper or siloed systems, Teamcenter integrates quality and compliance data across functions—design, engineering, production, and post-market. You get a continuous trace from idea to outcome.
- Design Data Management: Manage design inputs and outputs with digital twins.
- Product Line Management: Track Design History Files (DHF), Device Master Records (DMR), labeling, and UDI.
- Quality Process Management: Handle V&V, CAPA, change control, risk management, and document traceability.
Replace fragmented data with a centralized PLM/ALM environment:
- Seamless cross-functional collaboration
- International access and electronic signatures
- Regulatory workflows and approval tracking
| Benefit | Outcome |
| Improve Risk & Requirement Management | Maintain compliance throughout the lifecycle |
| Ensure DHF-DMR Continuity | Enable seamless design-to-production transitions |
| Enhance CAPA Processes | Link root cause, issues, and change management digitally |
| Enhance Product Quality | Prevent recurring issues and accelerate innovation |
| Boost Transparency | Get real-time visibility into all compliance data |
Teamcenter helps you avoid costly recalls and ensure global compliance by tracking data across:
Regulatory Information Management
Training & Qualification
Supplier Quality
Complaint Management
Electronic Records & Signatures