Hello,
I wan wondering if anyone could give a bit of guidance on using ATP swabs to validate our cleaning regime.
The factory is low risk, producing microbiologically stable products (largely oil based). Every batch is sent for a micro screen before distribution and they are normally all well within spec. The factory is BRC Grade A.
Currently, we take swabs from zones 1, 2 and 3 in production areas every 6 months, to validate the cleaning procedures (ie check that the cleaning SOPs in the factory are sufficient to keep any bugs under control.)
Swabs are done for TVC, enteros, e coli, yeasts and moulds, and Salmonella
limits are :
Max 1000 cfu/sq cm TVC
Max 10 cfu/sq cm enteros and e coli
Max 100 cfu/sq cm Y&M
Absence of Salmonella
I was looking at ATP because it would be cheaper and faster (currently a swab costs about £10 and takes 5 days for results) - on the last environmental sampling operation, there were quite a few areas that were well out of spec (mostly on TVC and/or yeasts) - which indicates that the cleaning SOPs need updating, (assuming the SOPs are being followed) it seems that getting an ATP kit would allow us to take many more samples, get a better baseline, so that we can identify what effect any new cleaning procedures have / identify any parts of equipment that are being missed.
I was wondering if by replacing the micro swabs with ATP swabs would I be straying into verification of the cleaning rather than validating the procedure... would an auditor be OK with using ATP for enviromental sampling? ![]()
Also, I've read that ATP correlates with bacterial presence, because it identifies cells... but if I've understood correctly a high ATP could mean high bacterial load, but a low ATP reading absolutely means low bacterial load...?
Thanks for your help
Tom







