QAD in Life Sciences
Many life sciences manufacturing sites around the world have deployed QAD Enterprise Applications (MFG/PRO).
Companies ranging from start-ups to multinationals enjoy the simplicity, reliability and performance that QAD delivers.
QAD developed the Life Sciences Edition to meet the needs of its worldwide customers in a variety of segments from medical devices to pharmaceuticals. QAD’s commitment to life sciences ensures medical device, pharmaceutical, and biotechnology manufacturers are able to work towards becoming effective enterprises, while meeting stringent regulatory demands.
QAD‘s solution supports flexible business process configuration and multiple business entities and can be deployed in multiple languages. Deployment options — including on demand — support the needs of global life science companies.
QAD’s solution supports critical quality requirements, including regulatory compliance, CAPA, and Device History/Electronic Batch Record requirements as well as providing a full range of Current Good Manufacturing Practices (cGMP) validation capabilities and tools. Enhanced controls and audit capabilities, along with eSignature support, help meet the mandate of compliance tracking.
QAD Enterprise Applications for Life Sciences:
- Full IQ/OQ/PQ Validation Support
- Integrated Device & Batch History Report (DHR)
- Robust Cradle to Grave Lot Traceability
- Intuitive and Easy to Use Interface
- FDA Regulatory Compliance
- Qualified SaaS Environment
- Built in Industry Best Practices & Processes
- 21 CFR part 11 Compliant
Web-based ERP Software – for Life Sciences
QAD is committed to helping manufacturers in the Life Sciences Industry. Another way QAD has made organisations more effective is through web-based ERP Software - QAD On Demand. This web-based ERP solution allows Life Sciences companies to focus on their business, not their software. The online functionality of QAD ERP software greatly reduces the cost of implementation and need for IT maintenance.
QAD On Demand Life Sciences Edition offers the same capabilities as the On Demand General Edition, but provides a qualified environment and the necessary standard operating procedures (SOPs) required to gain Food & Drug Administration (FDA) and current Good Manufacturing Practices (cGMP) validation.
