Medical Device eBMR Software
Our eBMR software streamlines the manufacturing process, enhancing efficiency and compliance. With user-friendly interfaces, it simplifies quality management while providing real-time data insights. Let this powerful tool elevate your production capabilities and ensure top-notch standards in medical device manufacturing.
ISO 13485 Compliant
MDR 2017 Compliant
21 CFR Part 11 Compliant
Automated Documentation
Complete
Traceability
Audit Ready
Regulatory Compliance
From Raw Materials to Finished Goods
From raw material requests to finished goods in storage, Rapidfacto streamlines every step. Say goodbye to paper-based bottlenecks and welcome a fully automated workflow that keeps your manufacturing documentation audit-ready and your team in sync.
Easily raise and track requests for raw materials with real-time inventory visibility.
Record and verify material issuance to maintain accurate stock levels and reduce waste.
Automate production workflows, ensure compliance, and keep everyone aligned on progress.
Monitor quality at every stage to catch issues early and maintain consistent product standards.
Verify your final products meet all specifications before sending them to the next stage.
Seamlessly move approved products into storage or shipping with complete traceability.
Contents of Rapidfacto eBMR
1. Raw & Packing Material Request
Create requisition slips from Production to Store Department
2. Raw & Packing Material Issuance
3. Manufacturing Steps Performed
4. IPQC (In Process Quality Control)
5. Finished Good Testing
6. Product Transfer to Store