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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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Life Sciences Functional Benefits

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