Allergen Cleaning Validation
Hi everyone,
Hope you are all doing great! I am currently in the process of validating our cleaning by swabbing for allergens, specifically eggs, since we produce vegan and non-vegan products. I am not quite sure how to proceed with the swab tests. From my understanding, this cleaning validation is done to ensure that the cleaning is properly done by our employees and that no egg residue is present on the working surfaces. This leads me to do my swabbing tests after the employees are done with the cleaning at the end of the day.
On the other hand, I've also been told that I should supervise the employees cleaning the surface before doing the swabbing to ensure that the cleaning is properly done. My only concern is that if I am there to supervise them, I will be incline to guide them if they are not following the cleaning procedures. If that happens, a result showing no allergen detected would not necessarily be accurate and representative of day-to-day cleaning (when I'm not there to watch them).
My question to you is: should I supervise the employee(s) doing the cleaning before I do cleaning validation swabbing tests (allergen or microbiological)?
Supervise when they are in training phase.
I would not be watching them every time this activity occurs unless it's a procedural requirement. Trust your employees.
What swabs are you using? In my mind allergen swabs isn't validation of cleaning, am I off? Like protein swabs, ATP, something like that would be better, no?
Perhaps that's what you're doing, but you said you're swabbing for eggs..... clarify?
What swabs are you using? In my mind allergen swabs isn't validation of cleaning, am I off? Like protein swabs, ATP, something like that would be better, no?
Perhaps that's what you're doing, but you said you're swabbing for eggs..... clarify?
Sorry if I was not clear, but we do protein swabs that we send to an external lab.
Sorry if I was not clear, but we do protein swabs that we send to an external lab.
Man, you send protein swabs out to external? How does that work? Do you not run until you have results? Or do you have to have product on a positive hold release plan?
I couldn't do this at my place, would take too long. We use the hygenia protein swabs, they get you feedback in under 10 minutes....
Man, you send protein swabs out to external? How does that work? Do you not run until you have results? Or do you have to have product on a positive hold release plan?
I couldn't do this at my place, would take too long. We use the hygenia protein swabs, they get you feedback in under 10 minutes....
Oh, I never heard about Hygenia swabs before. I will most certainly give it a look! Thanks.
Oh, I never heard about Hygenia swabs before. I will most certainly give it a look! Thanks.
https://www.hygiena....sidue/pro-clean
Oh for sure, check these out. Will make life easier and cheaper.....
The external lab testing using ELISA is more sensitive than rapid swabbing so as part of validation, that's the method you should use.
The method we established as best practice was as follows:
Test the product containing the allergen (this is to confirm the allergen can be recovered from the product matrix, that's not necessarily a "given"). Swab the dirty surface (again to check the allergen can be recovered with a swab). Normally we chose 3-6 difficult to clean places on equipment, depending on how complex it is.
Then check the team follow the method as written. Swab the surfaces again in triplicate and sample the first product made with the machine.
Repeat all three times over. That is your validation unless your machinery changes or equipment changes. Normally though we repeated it yearly because equipment surfaces can deteriorate. The "dirty" and spiked samples are important for recovery but also to make sure you're testing for the right protein. For eggs you will have different proteins in yolk and white for example. Milk there are choices about what to test for as well which differ on if it's say milk or cheese.
This should be validation ie before the product is launched (even if the FDA allow it to be later, they're wrong). If you're going back and doing it later, I can understand the concern of the delay in test results; then you have one of several options:
- Take the risk of the product being in market with pending allergen tests.
- Put the product on hold until test results are confirmed (you can get them in 24 hour turn around time but they cost a lot of money)
- Use rapid swabbing as suggested above to give you some level of comfort about putting the product on the market.
I would lean towards the second option. Remember it's only the vegan product which would need to go on hold and potentially depending on your process, you could use a small batch for this. An ideal time would be during the trial process as you're doing factory scale up.
There is a big but.
Here it is:
BUT
Rapid swabbing needs to be validated for the recovery from the matrix it's being found in. Even then it's not as accurate as ELISA which is quantitative.
Elisa is absolutely a method for validation. I would be tempted to use rapid swabbing if I was making a free from claim or an implied free from claim (like vegan, even though it doesn't mean free from, people think it does). But only as a gross indicator and also as some due diligence. It is absolutely not good enough for validation. Some of these companies will quote ppm sensitivity but genuinely question them on "how much is it in my product" and I can tell you now, if they say they know they aren't telling you the truth.
The external lab testing using ELISA is more sensitive than rapid swabbing so as part of validation, that's the method you should use.
The method we established as best practice was as follows:
Test the product containing the allergen (this is to confirm the allergen can be recovered from the product matrix, that's not necessarily a "given"). Swab the dirty surface (again to check the allergen can be recovered with a swab). Normally we chose 3-6 difficult to clean places on equipment, depending on how complex it is.
Then check the team follow the method as written. Swab the surfaces again in triplicate and sample the first product made with the machine.
Repeat all three times over. That is your validation unless your machinery changes or equipment changes. Normally though we repeated it yearly because equipment surfaces can deteriorate. The "dirty" and spiked samples are important for recovery but also to make sure you're testing for the right protein. For eggs you will have different proteins in yolk and white for example. Milk there are choices about what to test for as well which differ on if it's say milk or cheese.
This should be validation ie before the product is launched (even if the FDA allow it to be later, they're wrong). If you're going back and doing it later, I can understand the concern of the delay in test results; then you have one of several options:
- Take the risk of the product being in market with pending allergen tests.
- Put the product on hold until test results are confirmed (you can get them in 24 hour turn around time but they cost a lot of money)
- Use rapid swabbing as suggested above to give you some level of comfort about putting the product on the market.
I would lean towards the second option. Remember it's only the vegan product which would need to go on hold and potentially depending on your process, you could use a small batch for this. An ideal time would be during the trial process as you're doing factory scale up.
There is a big but.
Here it is:
BUT
Rapid swabbing needs to be validated for the recovery from the matrix it's being found in. Even then it's not as accurate as ELISA which is quantitative.
Elisa is absolutely a method for validation. I would be tempted to use rapid swabbing if I was making a free from claim or an implied free from claim (like vegan, even though it doesn't mean free from, people think it does). But only as a gross indicator and also as some due diligence. It is absolutely not good enough for validation. Some of these companies will quote ppm sensitivity but genuinely question them on "how much is it in my product" and I can tell you now, if they say they know they aren't telling you the truth.
Thank you for your comprehensive response! Gave me much more clarity on this matter.
Hi everyone,
Hope you are all doing great! I am currently in the process of validating our cleaning by swabbing for allergens, specifically eggs, since we produce vegan and non-vegan products. I am not quite sure how to proceed with the swab tests. From my understanding, this cleaning validation is done to ensure that the cleaning is properly done by our employees and that no egg residue is present on the working surfaces. This leads me to do my swabbing tests after the employees are done with the cleaning at the end of the day.
'Validation' and 'verification' sometimes get thrown around incorrectly in our industry. A 'validation' of cleaning is usually done for new setups and annual/quarterly check that your methods are effective. Validation normally relies on your daily swab tests tied into a more robust set of lab verified swabs. Your daily 'verification' is normally some type of rapid swab (as some indicated above) which means you aren't losing time waiting for a lab to return a clear result.
On the other hand, I've also been told that I should supervise the employees cleaning the surface before doing the swabbing to ensure that the cleaning is properly done. My only concern is that if I am there to supervise them, I will be incline to guide them if they are not following the cleaning procedures. If that happens, a result showing no allergen detected would not necessarily be accurate and representative of day-to-day cleaning (when I'm not there to watch them).
My question to you is: should I supervise the employee(s) doing the cleaning before I do cleaning validation swabbing tests (allergen or microbiological)?
If the training is up to date, and you've got confidence that the cleanings are being done correctly, doing it at random is best. But I get that cleaning is hard: sometimes the crews slack off, sometimes it's just difficult to really get into nooks and crannies. That's why we verify the hard-to-reach spots with rapid tests, and that's why post/pre-op inspections are so important.
Now, if you're out of control and failing your pre-op inspections left and right, you probably want to closely watch the cleaning before you do your validation swabs. When that comes back clean, you tell the crews the way they cleaned in front of you is the gold standard and you expect them to do it each time. Make sure they know the harm from egg allergens they can cause if they screw up. Then go in a few days later unannounced and do another set of lab swabs for further validation. Then do it again. 3 total sets of lab swabs with at least two pulled unannounced will tell you whether your cleaning methods and personnel are effective.
Gave some thoughts to the direct question in bold above. But generally, I'm with the others who are saying that the lab swabs should be reserved for this validation. I'm hoping you have a more readily available rapid test of some kind to use on a day to day verification basis.
But once you've completed the validation, paired with some good basic practices like sequencing (running the non-allergen products first after each cleaning) can help save on the costs of daily allergen testing for changeovers.
To answer your question about supervising the employees during the cleaning process, I would say no, don't supervise them.
We do our allergen validation once a year, and we swab before cleaning (to prove the allergen is there) and then after the employees have cleaned the equipment. We use the agri-test strips from Romer labs.