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 February 22, 2012  
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Solution News
Suite 2000 Version V3.70
 
The new release of Suite 2000 V3.70 is now available. This version has new SPC Enhancements and includes a new template pack for ISO 22000 : 2005.
 

Desktop Web Access Version V6.06
 
Expand the availability of your document collections, without sacrificing any of the document control that you depend on Suite 2000 to deliver. Desktop Web Access is a browser based user interface that lets your document consumers view, print and copy documents from your Suite 2000 document collection.
 
V6.06 includes the same security and document viewing abilities as Suite 2000 V3.60.
 
 

Conformance Series

 
Conformance Series Screen Shots
Click on the Screen Shot to see explanation
 

The Powerway Conformance Series is our solution group that enables the documentation of business processes and controls necessary to meet customer expectations and conformance to industry standards. It leverages the Suite 2000 platform, which means document control is built right in. Investing in Suite 2000 and the Powerway Conformance Series insures that your organization will be effectively working toward your conformance goals.

Role
Benefits
Audit Program Manager
Gives them the tools they need to make sure your company gets registered for your business critical standards, on time and within budget.
Quality
They need to be able to to find and author audit ready documentation, and insure that the rest of the organization is doing these things as well.

The Powerway Conformance Series currently supports the following standards;
  • ISO 9001:2008 - Quality Management Systems - Requirements
  • ISO/TS 16949:2002 - Quality management systems -- Particular requirements for the application of ISO 9001:2000 for automotive production and relevant service part organizations
  • ISO 14001:2004 - Environmental management systems -- Requirements with guidance for use
  • AS9100 - Quality Management System for Aerospace
  • AS9102 - First Article Inspection (FAI)
  • AS9103 - Variation Management of Key Characteristics
  • ISO 13485:2003 - Medical Device Quality Management System Requirements for Regulatory Purposes
  • ISO/IEC 17025:2005 - General requirements for the competence of testing and calibration requirements
 
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