Knowledge and skills transfer is an critical component of a successful health service.  Formal operating procedures and protocols must be captured and shared to deliver this expertise. Control of document distribution, its automated approval/issue and comprehensive records of change are essential in this process as the cost of failure is potentially huge in both human and financial terms.

Pharmaceutical and Medical Device businesses face similar, huge pressures. Regulatory compliance makes bringing products to market quickly, decreasing cycle time and increasing productivity hugely difficult.  The complexity and cost of complying with FDA regulation can place a massive drain on financial and human resources.

 

Qualsys and the Healthcare Industry

Qualsys EQMS application provides controlled distribution of Standard Operating Procedures (SOPs) and other important documentation with the aim of minimising the potential for human error.

• EQMS can dramatically reduce the cost and effort required to comply with Department of Health guidelines on Good Laboratory Practice. 

• EQMS allows Pharmaceutical organisations and platform for compliance to FDA 21 CFR Part11 and .  It also assists manufacturers of medical devices to comply with cGMP.

• EQMS can dramatically reduce the cost and effort required by Pathology departments to comply with CPA standards.

Organisations such as Bradford Hospitals NHS Trust have adopted EQMS to provide controlled distribution of important documentation with the aim of minimising the potential for human error.

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