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Medical Devices

 

Medical device companies use a number of different systems to demonstrate compliance with FDA or ISO requirements. These systems are responsible for sustaining processes like supplier selection, corrective and preventive actions or inventory management. An appropriate quality system has to be implemented, maintained and audited.

 

Clarmon’s solutions reduce the cost of compliance management in the medical device industry by automating recurring tasks and connecting all relevant processes. Quality records can be identified and retrieved instantly in case of inspections.

 

Connecting content across separated documents and instantly displaying change impact ensures that all regulatory information is maintained up-to-date.

Medical device companies gain a significant competitive advantage by eliminating the routine manual tasks, connecting and integrating compliance processes.

 

Upgrades to the quality system, which are necessary to improve performance, can be implemented and documented easier and faster.


 

Clarmon’s solutions help medical device companies:

 

 

 

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