Improve compliance and quality with connected product lifecycle management
See how our solutions support end-to-end traceability and continuous improvement
Medical device manufacturers face increasing pressure to meet strict regulatory standards while maintaining speed and innovation. This self-guided demo shows how integrated product lifecycle management (PLM) helps streamline product development, improve traceability, and reduce risk.
What you will learn in this demo:
Manage design changes efficiently
Enable continuous product improvement with structured change control processes that connect engineering, quality, and regulatory teams.
Automate design traceability through risk analysis
Ensure complete visibility across product data and design decisions, linking risk analysis directly to requirements and verification.
Strengthen quality with corrective and preventive actions (CAPA)
Identify and resolve quality issues early using a closed-loop CAPA process to reduce clinical and legal risk.
Accelerate regulatory compliance with design file management
Simplify regulatory submissions by managing all required documentation in a central, structured repository.
Streamline labeling and UDI management
Leverage built-in tools to manage Unique Device Identification (UDI) and labeling processes in alignment with global standards.
Explore how our solutions can help you bring safer, compliant medical devices to market—faster and more efficiently.