Webinar Replay: Managing FDA Medical Device Compliance in Windchill

Webinar Replay: Managing FDA Medical Device Compliance in Windchill

View this webinar replay to explore how to Manage FDA Medical Device Compliance in PTC Windchill: Medical device manufacturers have an arduous process of managing all the relevant data (documents, BOM’s, drawings, ECN’s, etc.) of the DHF, DMR, DHR to ensure passing audits for FDA medical device compliance See how Tristar is taking Continue reading

A Simplified Approach to Managing Medical Device History in Windchill

A Simplified Approach to Managing Medical Device History in Windchill

Are you relying on staff to complete Design History File (DHF) checklists? Are you relying on staff to maintain document lists and Device Master Record (DMR) binders? Are you having a difficult time complying with FDA 21 CFR Part 820? We offer a solution that simplifies device history management and Continue reading