QPack Requirements management tool is meant for the crucial software-development function of keeping requirements well tracked and controlled. Often, the requirements` creep is a make or break situation for a real-life software project. QPack Requirements Management will meet the organizational needs of a small unit or an enterprise equally well. This can act as the central element in managing a software project through the complete life-cycle. This tool makes it possible to work in distributed development environment, and the collaborative tool included will let you share your thoughts easily with your team members. You are able to capture, plan, approve, trace and validate your requirements centrally from a single repository. It will be possible to support the stringent regulatory requirements of medical device software development needs. Full audit trail and electronic signatures can be maintained, and compliance demonstrated easily.
Real-time dashboards can be set up and alerts and notifications generated to project stakeholders. This can help everyone remain in sync. End to end traceability can be maintained and analyzed. Requirements maintenance calls for heavy-duty editing, and this could be done with the most familiar environment of the MS Word. You can create content such as system requirements document, or detailed design in Microsoft-Word and synch it with QPack requirements tree. You would be able to use the unique document generator tool to easily design and generate documents, including embedded reports. These could be submitted to the database with just one click. It will be easy to synchronize changes. Embedding dynamic data in generated documents, such as requirements traceability matrix, charts, FMEA table, etc. is easily done. Traceability tool will help manage the traceability matrix. This is a very good tool.