Brendaisab
Registered
Hello All,
We (Medical Device manufacturer) have tons of paper records. To reduce the amount of "old" physical paper records we would like to scan the originals and store the documents electronically. Once the originals are scanned/stored electronically, we would like to destroy the originals.
Is there a ISO standard on the requirements or maybe an FDA guidance on how to do this? I'm guessing we would have to apply a certification e-signature on the scanned record stating it's a true and accurate copy of the original.
FDA 820.40 Document Controls section doesn't address the conversion of paper to electronic records and the destruction of the paper version. Neither does ISO13485 Sec 4.2.4 & 4.2.5
Could anyone point me in the correct direction? Or is this not acceptable practice?
We (Medical Device manufacturer) have tons of paper records. To reduce the amount of "old" physical paper records we would like to scan the originals and store the documents electronically. Once the originals are scanned/stored electronically, we would like to destroy the originals.
Is there a ISO standard on the requirements or maybe an FDA guidance on how to do this? I'm guessing we would have to apply a certification e-signature on the scanned record stating it's a true and accurate copy of the original.
FDA 820.40 Document Controls section doesn't address the conversion of paper to electronic records and the destruction of the paper version. Neither does ISO13485 Sec 4.2.4 & 4.2.5
Could anyone point me in the correct direction? Or is this not acceptable practice?