Hi all, Are you aware that there is an open consultation regarding the implementation of 'safety features' under the falsified medicines directive- a copy of the proposed legislation is on the gov.uk site, it will apply in UK law from 9th Feb 2019.
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Hi all, Are you aware that there is an open consultation regarding the implementation of 'safety features' under the falsified medicines directive- a copy of the proposed legislation is on the gov.uk site, it will apply in UK law from 9th Feb 2019.
Thanks- does this mean we would need to record the individual identification number of each product, not just the batch number? :(
This is only possible if the manufacturer provides a barcoded label.
If this is the case, some of our LIMS would need modifying to allow both batch number and unique identifiers???:(:(:(
Some more info and advice would be great please on how this could affect Blood banks storing products/ meds.
many thanks
unsure I’m still figuring this one out will get back to you