Hi all SQF experts, so i was reviewing 2.3 contract service providers policy (which i did not write, it was the previous administration) and as a requirement asks for accreditation from ISO 17025 (which I'm aware that its a requirement from the code) and also to be registered with the FDA now this I have not idea where it came from (as i said i didn't write this policy) so my question is do any of you guys have and auditor asking you for FDA registration from your lab? Does FDA requires laboratories to be registered with them? please help me get some enlightenment on this.
Thanks.
Brenda