The Design History File (DHF) is your ticket to improved medical device quality and streamlined regulatory compliance. Many companies make costly and time-consuming errors when creating their DHFs, leading to longer than necessary audits and inspections.
Avoid these mistakes, and you’ll minimize lost time and unnecessary costs getting to market.
Join leading product development organizations Quality Centric Consulting and Jama Software for a webinar in which you’ll learn:
- The top DHF errors that are costing you money
- How to tackle 21 CFR 820.30 requirements
- How Jama Connect™ streamlines the DHF process