SteriPack,a supplier of cleanroom sterilized packaging solutions for medical devices,is extending the usage of QAD's Enterprise Applications Life Science Edition at its new facility in the US.
Previously,SteriPack has also implemented the Enterprise Applications at its facilities at Ireland,Poland and Malaysia.
Designed for use in single-or multi-site operations,QAD Enterprise Applications are available in multiple languages with true multi-tiered on-premise QAD On Demand software as a service(SaaS)and hybrid deployment options.
QAD Enterprise Applications also support critical quality requirements including regulatory compliance,CAPA,and Device History/Electronic Batch Record requirements.
In addition,QAD offers enhanced controls and audit capabilities,along with eSignature support to help meet the mandate of compliance tracking.
QAD sales and marketing EMEA vice president Steve Gardner said,"QAD Enterprise Applications and QAD On Demand give medical device manufacturers a flexible,cost-effective global ERP solution to help them bring their products to market on time,while meeting regulatory requirements and managing risk."
SteriPack USA president Tony Paolino said,"Extending QAD to SteriPack USA enables us to rapidly onboard new operations that can run at peak performance to deliver consistent supply to our medical device customers."
