In Reply to Parent Post by JennyGernon
I was interested to see how you all manage your microbiology process. We currently process our microbiology as follows
test lenses every 6 months, write up Process Validation Report. Confirm if there are any non conformances or not.
I recently had a tech file review and was advised that I need to include information in our tech file on bioburden. I keep this separately at the moment and was interested to see if others put microbiology information in their tech files.
Hello Jenny and welcome to the Cove
A lot of context is missing. "Microbiology process" can be many things. What does your org do? From your post I gather you manufacture some medical devices. Is that correct? Are those sterile medical devices? Were you referring to a NB audit?
The more context you provide, the higher the chances you will get useful responses (though it's not guaranteed...)