Quality Management with QSi System 9000
Do you face these challenges?
- Compliance issues with your ISO 9001:2000 certification due to incomplete or out-of-date Quality Manual documentation?
- Inefficient process for document creation and approval of your Quality Manual?
- Lack of structured processes for internal quality audit, escalation, and corrective action?
- No control of critical due dates and deadlines with authorities?
Then QSi System 9000 is for You!
Since 1997, Computacenter’s Application Services team has been distributing QSi System Series from IBS America. IBS continuously develops and refines solutions that solve compliance management problems. The flagship product, QSi System for Quality Management, incorporates more than ten years of enhancements developed along with Corporate users on a global level.
The extended product family includes
• QSi System for Quality Management,
• QSi System For Automotive Quality Management,
• QSi System for Environmental Management,
• QSi System for FDA Document Control
With over 1,200 systems installed worldwide, in eight different languages, QSi is the leader in the field.
QSi System for Quality Management
The QSi System for Quality Management will help your organization reap the promised benefits of ISO 9001:2000 certification including improved customer satisfaction and lower costs.
The QSi System for Quality Management integrates modules that address the following sections:
Document Control
The Document Control modules provide all the templates and examples needed to complete a well-structured Quality Manual and to create Procedures, Work Instructions, Specifications and Quality Plan documents. Features include multi-level access security, electronic signatures, revision control and automated document status update. Document review and approval workflow across the network, can be either serial or parallel. Each document contains a complete, automatically generated history and document archiving is automatic.
Audits and Corrective Actions
Internal Assessment and Supplier Assessment Modules each provide company auditors a 350+ question audit program. There is push button connection from the Internal Assessment module to the Corrective Action Request (CAR) module for the creation of CARs and from the Supplier Assessment module to the Supplier Management module for the creation of SCARs. This helps to complete the audit findings/corrective action process. The CAR module is the company-wide corrective and preventive action system. The Escalation feature ensures that requests turn into action.
Quality Records
The Quality Records section contains fourteen modules designed to ensure the accuracy, availability and safety of the records which demonstrates that a quality system is working properly. Modules use ISO 9001:2000 ready entry forms and include push button connections to easily manage workflow. Critical due dates are monitored by Escalation Control which sends messages of missed deadlines to responsible authorities.
Reference and Planning
The Reference and Planning section includes modules to assist users in planning and implementing a compliance management system. An indexed and searchable ISO 9001:2000 knowledge base provides specific implementation solutions. A Project Task Management module enables the creation of project tasks, project action items, and project notes for task assignment and feedback and a discussion module serves as a forum for network-wide, interactive communication.
QSi System For Automotive Quality Management
The QSi System for Automotive Quality Management is designed to meet the requirements of ISO/TS 16949:2002. Since ISO/TS 16949:2002 is built on the foundation of ISO 9001:2000, the QSi System for Quality
QSi System for Environmental Management
The ISO 14000 environmental standard shares a number of common management system principles with the ISO 9001:2000 series of quality system standards and contains a suite of 12 additional specific environmental management modules. The most important of these deal with Environmental Aspects and Impacts, Objectives and Targets, MSDS and Hazardous Materials, Emergency Preparedness, and a Register of Legal Requirements.
QSi System for FDA Document Control
The QSi System for FDA Document Control provides all the templates and examples needed to complete a well-structured Quality Manual and to create Procedures, Work Instructions, Specifications, Quality Plans and Process Description documents.
Contact us at: infobelgium@computacenter.com or infolux@computacenter.com to know more about our offering.