Q-Pulse^® Document Control Software 5.2

Version 5.2 now available, featuring new interface and functionality, as well as options for meeting FDA CFR 21 Part 11 Requirements.

Q-Pulse is a market-leading, Windows-based application for managing class Document Control, corrective action and many other quality assurance issues necessary for compliance to ISO 9001:2000, ISO 14000, QS 9000, ISO/TS 16949, JCAHO, FDA or other similar regulations. Q-Pulse Document Control Software extends beyond controlling documentation or demonstrating system compliance, its integrated tools promote solutions to improve business efficiencies by:

• Encouraging ownership of the compliance management system,
• Reducing bureaucracy of compliance management,
• Delivering improvement in bottom-line performance.

Document Control Software Features

• Q-Pulse Document Control Software Overview
• Automates tedious, time consuming tasks
• Computerized and/or Printed Reports
• Developed for managing QA-by experienced QA managers
• Reduces the overhead of managing ISO 9001:2000
• Password Protection to maintain System Integrity
• Security
• Low cost of ownership

• Q-Pulse Document Control Software includes these integrated modules:
• Document Control
• Non-Conformance; Corrective & Preventive Actions
• Auditing
• Customer Management
• Analysis and Improvement
• Supplier Control
• Asset Management
• Training & Competence
• Workload Management
• Reduces the overhead of managing ISO 9001:2000
• Automates tedious, time consuming tasks
• Security and System Integrity
• Low cost of ownership
• Optional FDA CFR 21 Part 11 Features

See also:

• PowerPoint demonstration of feature benefits.

• Help System and Step-By-Step User Manual
• Training is available through seminars or on-site at your location
• 30-day satisfaction guarantee
• Annual Support Agreement Available