• Development of Qualification Protocols for Equipment & Automation
  • Standard Operation Procedures (SOP) for Process and Quality Control
  • Factory Acceptance Test
  • Site Acceptance Test
  • Development of DQ, IQ, OQ and PQ Documents
  • Review and Develop User Requirement Specification (URS)
  • Review of Functional Design Specification (FDS) of equipment
  • Qualification Schedule
  • Quality Management System
  • Validation Master Plan (VMP)
  • Equipment Validation
  • Utility and Facility Validation
  • Computer System Validation
  • PLC HMI and Automation Validation
  • Risk & Impact Assessment