QAD in Life Sciences
Over 400 life sciences manufacturing sites in more than 60 countries around the world have deployed QAD Enterprise Applications. 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 the cloud — 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 Lets You Work Faster, Work Smarter:
- 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
Cloud ERP Software – for Life Sciences
QAD is committed to helping manufacturers in the Life Sciences Industry. Another way QAD has made organizations more effective is through our web-based ERP Software - QAD Cloud ERP. This cloud-based ERP solution allows Life Sciences companies to focus on their business, not their software. The online functionality of our ERP software greatly reduces the cost of implementation and need for IT maintenance.
QAD Cloud ERP Life Sciences Edition offers the same capabilities as the 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.
QAD recognizes the trust that our customers place in us as their Enterprise Resource Planning solution provider. This is why so many Life Sciences companies have chosen QAD. Learn more.