Beyond Colored Folders and Spreadsheets: Next-Generation Document Control for the Medical Device Industry
Medical device manufacturers face unique obstacles in effectively managing and securely sharing their product information. Using colored folders and network drives for distribution, sign-off and storage of your device records could be putting your product at risk. Medical device document control is easier with the right systems in place. Medical device companies can efficiently maintain their records, confidently achieve compliance and speed time to market.
This whitepaper gives insight into how automated, electronic solutions can help medical device companies manage their device master record (DMR), design history file (DHF) and change orders easily and efficiently without extra validation overhead.
Related Medical Device Resources
The whitepaper Moving From Paper to Electronic Change Management: Five Key Issues to Consider as Your Company Addresses 21 CFR Part 11 provides guidelines for meeting FDA regulations while moving from a paper based system to an electronic system.
Learn how Arena can help medical device companies better manage their device master records (DMRs), design history files (DHFs) and achieve medical device compliance on our Medical Device Compliance page.
Additional Resources
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