Reporting and Compliance: Visure Requirements offers reporting capabilities that allow you to generate custom reports and metrics to monitor project progress, traceability coverage, risk status, and compliance with ISO 13485.This ensures that any changes made to the medical device development are properly evaluated, approved, and documented, aligning with ISO 13485 requirements. The platform supports change request tracking, impact analysis, and change control processes.
Requirements Management & Traceability with Microsoft Office Word and Excel.Optimizing for DO-178C & DO-254 Certification.Leveraging AI to Accelerate Requirements Management Process.Requirements AI- Course Online Training.Model Based Systems Engineering (MBSE) Online Training Course.