Why QMSTools? 10 Reasons
QMSTools System by System Justification
Document Development
Reduces time needed to develop customized quality policies and procedures for each location
Comprehensive quality system documents developed in hours versus weeks
Document Modification / Document Control
Reduces time spent maintaining documents and ensuring availability, ease of approval
No lost documents
Less paperwork
Fewer man-hours spent on maintaining accurate, controlled documents
Calendar
No missed time sensitive laboratory activities
Implementation
Reduces time spent developing quality system implementation plan
Ensures all system requirements deemed necessary by the user are identified and tracked
Training
Reduces time spent evaluating individual training needs
Reduces employee error by ensuring training stays current
No lost documents
Less paperwork
Quality Records
Reduces need for off-site storage
Reduces time spent locating and destroying documents
Action System
Reduces solution implementation time for problems identified in the laboratory
Minimizes attention needed by quality staff
Minimizes time needed to gather key information for meetings
Work Instruction
Reduces time and effort to modify and distribute changes to analytical test methods
Reduces time and effort to modify and distribute new instructions to technicians
Improves transfer of intellectual property between locations
Work Instruction Support
Reduces time establishing method related equipment and supply requirements
Internal Audits
Reduces time spent organizing audits (auditors / participants)
Reduces time spent identifying audit questions / audit scope
Reduces time needed to develop customized quality policies and procedures for each location
Comprehensive quality system documents developed in hours versus weeks
Document Modification / Document Control
Reduces time spent maintaining documents and ensuring availability, ease of approval
No lost documents
Less paperwork
Fewer man-hours spent on maintaining accurate, controlled documents
Calendar
No missed time sensitive laboratory activities
Implementation
Reduces time spent developing quality system implementation plan
Ensures all system requirements deemed necessary by the user are identified and tracked
Training
Reduces time spent evaluating individual training needs
Reduces employee error by ensuring training stays current
No lost documents
Less paperwork
Quality Records
Reduces need for off-site storage
Reduces time spent locating and destroying documents
Action System
Reduces solution implementation time for problems identified in the laboratory
Minimizes attention needed by quality staff
Minimizes time needed to gather key information for meetings
Work Instruction
Reduces time and effort to modify and distribute changes to analytical test methods
Reduces time and effort to modify and distribute new instructions to technicians
Improves transfer of intellectual property between locations
Work Instruction Support
Reduces time establishing method related equipment and supply requirements
Internal Audits
Reduces time spent organizing audits (auditors / participants)
Reduces time spent identifying audit questions / audit scope
User-friendly system minimizes effort to maintain an organized, cohesive quality system.
Web-based improves access and transparency.
Allows the laboratory to benefit from the structure and discipline of a quality system without becoming consumed by the operation and maintenance of the system.
Knowledge-based system that ensures implementation to specific and/or customizable quality standard.
Reduces development time for system implementation.
Minimizes liability associated with data quality.
Handy maintenance / electronic storage of quality records needed to support analytical results audit trail.
Automatic scheduling and reminders for required tasks based on analytical method requirement.
More comprehensive than our competitors as it supports specific analytical test method requirement.
Great support from experienced professionals.