Quality Management System (QMS) Development

Document Your Processes and Corporate Intelligence

GBC supports the development, review, and enhancement of Quality Management Systems (QMS) and associated documentation including:

  • Company Policies
  • Standard Operating Procedures (SOPs)
  • Training Processes and Documentation
  • Clinical Trial Processes (Qualification, Initiation, Monitoring, Close Out)
  • Biospecimen Management Processes (Collection, Processing, Storage, Distribution)
  • Data Management Procedures
  • Material, Supply, and Equipment Specifications
  • Equipment Monitoring, Maintenance, and Calibration
  • Technical Work Instructions
  • Laboratory Instructions
  • Batch Records
  • Software Usage Instructions
  • Customer Service Processes
  • Operations Manuals
  • Process Deviations
  • Corrective Action and Preventive Action Procedures (CAPA)
  • Management Review

For additional information on GBC’s consulting services please contact consulting@globalbioclinical.com or register and send us your inquiry here.