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.