QPack is a comprehensive requirements management software that facilitates end-to-end product delivery by allowing you to monitor your requirements. It includes a Medical accelerator designed explicitly for medical device manufacturers, with compliance to IEC62304 and ISO14971.
QPack Requirements Management Tool is a versatile software solution that enables users to track requirements effectively and streamline product delivery. Whether you are a startup or a well-established organization, QPack has been designed to meet your specific needs.
By using QPack as the central hub for your entire product development lifecycle, you can accomplish several critical tasks, such as capturing, planning, validating, and approving requirements in a single repository. Additionally, QPack provides real-time collaboration tools that allow you to communicate and share your ideas with your team, regardless of your location.
Furthermore, QPack is ideal for enterprises that work in distributed development environments, as it supports stringent regulations that medical device manufacturers have to comply with, such as IEC62304 and ISO14971. With QPack, you get a one-stop-shop for end-to-end traceability and impact analysis of any ALM artifact, along with a full audit trail and electronic signature (part 11 compliant).
Finally, QPack provides real-time dashboards, alerts, and notifications that keep project stakeholders in sync and up-to-date. Also, you can work effectively in your native Office environment, making it an excellent choice for users who prioritize ease of use and convenience.
By using QPack as the central hub for your entire product development lifecycle, you can accomplish several critical tasks, such as capturing, planning, validating, and approving requirements in a single repository. Additionally, QPack provides real-time collaboration tools that allow you to communicate and share your ideas with your team, regardless of your location.
Furthermore, QPack is ideal for enterprises that work in distributed development environments, as it supports stringent regulations that medical device manufacturers have to comply with, such as IEC62304 and ISO14971. With QPack, you get a one-stop-shop for end-to-end traceability and impact analysis of any ALM artifact, along with a full audit trail and electronic signature (part 11 compliant).
Finally, QPack provides real-time dashboards, alerts, and notifications that keep project stakeholders in sync and up-to-date. Also, you can work effectively in your native Office environment, making it an excellent choice for users who prioritize ease of use and convenience.
What's New
Version 7.0: New traceability matrix tool, Fully supported on web, smartphones and tablets, available at Google store and Google Extension