Quality Management System (QMS) Development

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.