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QPack Application Lifecycle Management 5.2

QPack Application Lifecycle Management Requirements Software Solution by Orcanos


Last Week downloads: 0
Total downloads: 168
  • Last Updated: Nov 28, 2012
  • License: Shareware $66.00
  • OS: Windows Vista/2003/XP
  • Requirements: No special requirements

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4 out of 5 based on 1 ratings for QPack Application Lifecycle Management 5.2

For QPack Application Lifecycle Management 5.2Publisher's description


QPack Application Lifecycle Management is a Development software developed by Orcanos. After our trial and test, the software is proved to be official, secure and free. Here is the official description for QPack Application Lifecycle Management:

EditByBSEditor: QPack by Orcanos - the leading solution for Application Lifecycle Management - ALM 2.0 - Requirements Software Solution - for software developement and for medical devices development, medical software testing, medical device software validation. Complete and structured solution or a software project, from requirements definition, through design and specs to customer delivery - the complete Application Lifecycle Management solution. QPack is an end-to-end solution for Application Lifecycle Management, containing all development lifecycle modules, such as market requirements, system specs, development, testing, and delivery. QPack ALM supports the marketing team, system architects, developers and testers by providing each team with professional tools suited to its specific needs and methodologies. QPack is cost effective, easy to use and requires very little maintenance.

By using the requirements definition tool and release MANAGER, QPack ALM solution makes it possible to determine the PRECISE feasibility of new functionality and see the Impact of changes, all while taking into account the time constraints of release to market. QPack application lifecycle management solution for medical device provides a single repository of data management for medical device development, providing professional ALM tools for all parties involved with the medical device software development, including market requirements (MRS), product requirements (PRS), risk management tool according to the FMEA standard and validation and verification.

QPack for medical device software development supports compliance with the FDA regulations, providing the customer with an end-to-end solution for the medical device development process. QPack medical device software development provides the followings modules: Market requirements management (MRS) Product requirements management Electronic records and signatures Document control Audit trail Full traceability Validation and more.
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