Ditch your paper-based device history records and all the errors and inefficiencies that come with them. It’s time to take control of your DHR documentation.
MasterControl’s electronic device history record solution is a new breed of manufacturing application – data-driven, operator-centric, and fully connected. Medical device companies get a competitive advantage with MasterControl’s cost-effective, quickly deployable, easily integrated, and immediately impactful eDHR software. Find out how our end-to-end eDHR solution bridges the digital gap between core business and information applications and the shop floor personnel who drive the last mile of production.
Why settle for scattered paper documentation when you can electronically capture, store, analyse, and report on all your essential device history data? MasterControl eDHR software provides complete, accurate data capture and robust analytics and reporting capabilities so you can make better decisions faster.
Automated data integrity checks.
Enforced data limits and thresholds.
Right-first-time data.
MasterControl device history record software reduces the risk of production problems that are all too common with paper-based processes. With our eDHR software you can forget you ever worried about missing, incomplete, or illegible documentation or incorrectly logged data formats and units of measure.
Real-time deviation tracking.
Enhanced visibility and traceability.
Easy access to trending data.
Our electronic device history record software is designed to connect your standard operating procedures (SOPs), work instructions, training activities, quality events, and change control processes. It also integrates with other core systems, such as enterprise resource planning (ERP) solutions, for full visibility.
Complete, audit-ready eDHR forms.
Automated training tracking.
Robust collaboration tools.
The Ultimate Guide to Digitizing the Shop Floor
Contact us today to discover how MasterControl’s electronic device history record (eDHR) system empowers manufacturers to create and deliver an easy-to-audit record of proper handling for every step in the production of a medical device.
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