In order to bring you the best possible user experience, this site uses Javascript. If you are seeing this message, it is likely that the Javascript option in your browser is disabled. For optimal viewing of this site, please ensure that Javascript is enabled for your browser.
QAD Inc.


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.