A
antho10359
Is there a regulatory or compendial requirement to keep an actual physical representation of each medical device model or is the Device Master File containing the specifications adequate?
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I don't know what compendial means and I am not aware of a regulatory requirement, but it sure is sound business practice to keep an actual device.antho10359 said:Is there a regulatory or compendial requirement to keep an actual physical representation of each medical device model or is the Device Master File containing the specifications adequate?
Thanks