Aras Corporation

Changing PLM shouldn’t mean starting over. Teams keep familiar structures for items, BOMs, and change control, so the move brings minimal disruption. Protect years of investment in data, processes, and user expertise.

In medical device manufacturing, an engineering change rarely happens in isolation. Every change touches risk, quality, and manufacturing. Aras connects every change to its regulatory, quality, and manufacturing impact on one digital thread.

When a design changes, can you see every risk file, document, and supplier process it affects before you approve it? Aras shows the full impact of an engineering change across engineering, quality, and manufacturing.

Every product change reflected across engineering, quality, and production, without manual reconciliation. One connected product record.

Safer medical devices, to market faster. Connect product development, quality, and compliance through one digital thread.

Audit-ready documentation shouldn't mean rebuilding evidence by hand. Move from a static traceability matrix to live, end-to-end traceability.