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Life Sciences Functional Benefits

QAD life sciences edition supports critical quality requirements including corrective action/preventive action (CAPA) and adverse reaction reporting, and provides a full range of validation capabilities. QAD provides a suite of tools to assist in Current Good Manufacturing Practices (cGMP) validation, including advanced controls, audit trails and the use of eSignatures.

QAD Enterprise Applications solution addresses most aspects of a life sciences company’s business processes, including:

  • cGMP - Computer System Validation
  • CFR 21 Part 11 (21CFR11)
  • Manufacturing and Contract Manufacturing
  • Quality Management
  • Serialization & ePedigree
  • Forward & Backward Lot/Serial Tracking
  • WIP Lot Trace
  • EDI
  • Transportation Management
  • Customer Service and Support
  • Engineering Change Control
  • Contracts, Promotions, and Rebates
  • Demand Planning
  • Packaging
  • Supply Chain Portal
  • Regulatory Validation Compliance
  • Warehouse Management
  • Distribution

The process map below demonstrates the breadth of QAD’s life sciences offering.

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