Orcanos Released Qpack 5 Users' Free Edition Requirements Management And Alm For Small Teams
Orcanos (http://www.orcanos.com), the leading provider of Application Lifecycle Management (ALM) solutions, released the 5 user's free edition of QPack, a web-based Requirements Management system ( http://www.orcanos.com/compliance/products/requirements-management/) with Test Management and FMEA Risk Management modules, targeted for small-Medium software companies and medical devices manufacturers.
- (1888PressRelease) August 30, 2014 - Orcanos LTD, Israel - QPack provides an easy to use interface with a complete solution for managing projects, from concept definition through requirements design and testing, until customer support - a complete Application Lifecycle Management system.
Along with the ALM functionality, QPack Suite also provides the following modules:
- Service Center for customer support
- Document control with electronic signature.
"We believe that QPack is the ultimate solution for small-Medium businesses, as the QPack Suite provides all needed in order to manage development processes efficiently, from concept to customer support. Our unique medical extensions for medical device manufacturers make QPack unique in this field, providing document generation utilities that help preparing documents for submissions, and integrating the FMEA risk management and customer tickets/complaints to the requirements and testing procedures' says Rami Azulay, Orcanos VP Sales and marketing.
About Orcanos
Orcanos is a leading software vendor that provides QPack software solutions for ALM, Risk Management, Service Center and Document Control, specializing in the medical device industry. Orcanos has more than 8 years of proven experience in regulated hi-tech industry, working with software, electronics and medical device companies, assisting them in building their operational excellence.
While moving 80% of the manual paperwork into a process automation tool, Orcanos ensures significant reduction in R&D cost, and readiness for CE, FDA submission and audits for medical device manufacturers.
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