Organizations who use medical devices are subject to a number of regulations. Examples are regulations related to periodic maintenance, service, cleaning and sterilization. However, when an organization changes or combines medical devices further regulations apply.
Compliance with all these regulations can be burdensome when it is organized in a reactive and ad-hoc way.
Grey RA helps organizations to ensure compliance with a structured approach based on your own quality system. New or updated regulations are then only triggers to improve your quality system and no longer a reason to ring the alarm bells.
Interested? Contact Grey RA today for a free introduction in the possibilities.