Automating version management of medical device manuals! Achieving cost reduction in translation while ensuring regulatory compliance.

Automatically record approval flows and revision histories to enhance compliance. Achieve cost reduction through differential translation and rapid response to frequent revisions due to regulatory changes.

In the medical industry, where high safety standards are required, there is no room for compromise on "version control" and "audit trails" in manuals. 'IXIA CCMS' supports strict operations that eliminate human errors by visualizing the entire lifecycle of documents. 【Features】 ◎ Perfect Traceability: Automatically records "when, who, what item, and how it was modified" for each topic. Instantly generates reports of the history required for audits. ◎ Quality Control through Workflow: Enforces the drafting, review, and approval processes within the system. Physically prevents the risk of unapproved content being published. ◎ Ensuring Consistency Across Languages: When the source language (Japanese or English) is revised, automatically sets "update flags" for all affected translated language topics. Prevents accidents due to translation omissions. ◎ Rapid Response to Regulatory Changes: Allows for cross-application of modifications across all manuals in response to regulatory changes, significantly reducing revision costs and time to release. ＼For more details, please contact us or download the materials!／

Catalog and manual creation