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
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- Customer Service and Support
- Engineering Change Control
- Contracts, Promotions, and Rebates
- Demand Planning
- Packaging
- Supply Chain Portal
- Regulatory Validation Compliance
- Warehouse Management
- Distribution
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The process map below demonstrates the breadth of QAD’s life sciences offering.
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