KEY FEATURES

• Non-conformance Tracking and Analysis
• Corrective Actions
• Supplier Corrective Actions (SCAR)
• Safety Corrective Actions
• Preventive Actions
• Risk Management – FMEA and SWOT Analysis
• Internal audits
• Document Management Review Meetings
• Customer Satisfaction Surveys
• Email reports directly to employees
• Define user passwords and privileges

BENEFITS

• A vital software tool to ensure ISO 9001:2015, AS9100, ISO/TS 16949, API Q1 compliance
• Improve Customer satisfaction
• Build a simple and efficient Quality Management System (QMS)
• Paperless QMS
• Efficient and cost effective

Q-MED KEY FEATURES

• Nonconformance Tracking
• Corrective Actions (CA)
• Preventive Actions (PA)
• Audit management
• Risk Management – FMEA and SWOT Analysis
• Meeting management
• Project management
• Customer satisfaction surveys
• CFR21 part 11 compliant security, activity logs, audit trails
• User login: define user passwords and privileges

BENEFITS

• Complies with requirements of
  • ISO 13485
  • 21 CFR Part 820
  • ISO 9001:2015
  • AS9100
  • ISO/TS 16949
  • API Q1
• Provides a concise, electronic record of historical events, actions, and improvement
• Efficiently maintains quality records
• Improve product reliability and process performance
• Improve Customer Satisfaction
• Efficient and cost effective
• Simple Reports and analysis

KEY FEATURES

• Manage Training Records
• Define Job Descriptions / Roles and Responsibilities
• Define Training requirements
• Certification Requirements
• Re-Certification Requirements
• Document revisions trigger training requirements
• Email Reports directly to affected employees

BENEFITS

• Efficient and cost effective
• A vital tool to ensure ISO 9001:2015, AS9100, and ISO/TS 16949 compliance
• Build a simple and efficient Quality Management System (QMS)
• Paperless QMS

DOCUMENT CONTROL & EMPLOYEE TRAINING MANAGEMENT

• Complete document life cycle management
• Controls any electronic document including Microsoft office files: Word, Excel, PowerPoint, PDF, AutoCAD, SolidWorks
• Control document releases
• Ensure approvals are documented
• Organize Electronic Documents
• New releases reset training requirements
• Simple, effective reports
• Measure the effectiveness of your document control system
• Manage Training Records
• Define Job Descriptions / Roles and Responsibilities
• Define Training requirements
• Manage a Training Schedule
• Certification Requirements
• Re-Certification Requirements
• Document revisions trigger training requirements
• Email Reports directly to affected employees

BENEFITS

• A vital tool to ensure ISO 9001:2015, AS9100, and ISO/TS 16949, API Q1 compliance
• Efficient and cost effective
• Simple document life cycle management
• Build a simple and efficient Quality Management System (QMS)

KEY FEATURES

• Control of Calibrated Equipment
• Recall Report for “Out of Cal” Equipment
• Preventive Maintenance Schedules
• Track Unscheduled Maintenance
• Generate Fix-It-Tickets
• Control Miscellaneous Assets
• User login: define user passwords and privileges

BENEFITS

• A Vital Tool to Ensure ISO 9001:2015 Compliance
• Build a simple and efficient Quality Management System (QMS)
• Efficient and Cost Effective
• Paperless System

KEY FEATURES

• Develop Vendor qualification plans
• Record Vendor qualification results
• Maintain your Approved Vendor List (AVL)
• Establish criteria for selection, evaluation and re-evaluation of suppliers
• Link electronic files (paperless system)
• Rich set of reports
• User login: define user passwords and privileges

BENEFITS

• Build a simple and efficient Quality Management System (QMS)
• Comply with standard Purchasing requirements
• Efficient and cost effective
• A vital tool to ensure ISO 9001:2015, AS9100, ISO/TS 16949, API Q1 compliance
• Paperless system

KEY FEATURES

• Implement Risk based strategies for ISO 9001:2015
  • Identify failure modes for each process or item
    • Identify failure effects and severity
    • Identify causes and frequency
    • Identify current controls and detection levels
  • Develop multiple actions associated with this failure mode
    • Assign owners and due dates
    • Establish verification and validation criteria
• Electronic signature for management approval
• Rich set of reports
  • Track open actions and delinquent due dates

BENEFITS

• Save time and reduce the cost of compliance to Quality Standards such as ISO 9001:2015
• Implement Risk Based Thinking
• Easy to use
  • Collaborative platform
  • Simple, menu driven user interface
  • Easy to train users
• Convenient, intuitive forms
  • Can restrict users to control data integrity
• Rich set of reports
  • Easy to identify delinquencies, stalled actions
  • Reports may be emailed with a single click
  • Export data to Excel for further analysis

Note: All the features of the SBS FMEA Database are included in the SBS Q-Med Database and SBS Quality Database