Wednesday, January 15, 2014

QAD in Life Sciences

(Source: www.bsdinsight.com)
Over 400 life sciences manufacturing sites in more than 40 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 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.

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