Improvement Systems

  • System Design & Implementation
  • Documentation & Reporting
  • Product Quality Complaint Investigation
  • Adverse Drug Event Reporting
  • Drug Product Recall Program Development
  • System Design & Implementation
  • Investigation & Root Cause Analysis
  • Quality Systems Development
  • Finished Product Risk Assessment

 

  • Internal Audit Program Development
  • Regulatory Inspection Preparedness
  • Mock Audits/Inspections
  • Remediation Assistance
  • Audit Support & Advisory Services
  • Investigation & Mitigation Processes
  • Continuous Quality Improvement
  • Data Review & Analysis
  • System Design & Implementation
  • CAPA Risk Assessment
  • Effectiveness Evaluation
  • System Design & Implementation
  • Document Change Control
  • Process Change Control
  • Equipment Change Control
  • Material Change Control

Speak to our consulting specialists at
314.241.0213 or email consulting@dynalabs.us