Validation and contineu verification

As per new guidlines of us fda, every product not only need to validate but also need to verify this process contineusly for consistant quality product manufacturing.

But we varify the all parameter of manufacturing all batch by APQR “anual product quality review”. This is also continues varification method, there is any other way to explain we regularly check and verify the parameter? ?

How can we explain this?

regards,

Abhijeet