Similarly, whereas critical limits are then assignable for CCP's , monitoring limits would be assignable for OPRP's and both would have correction, corrective action and verification requirements.
So by way of example my product is chocolate , a screen is being used to control metallic FM, the rationale for calling it an OPRP is what?, the monitoring limit or requirement is what?, if there is failure at this step , the correction step is what?, etc.
I am thinking that for the auditor or assessor coming in checkout the facility summary tables would exist showing the derivation of each CCP and OPRP respectively.
7.5 Establishing the operational prerequisite programmes (PRPs)
The operational PRPs shall be documented and shall include the following information for each programme:
a)food safety hazard(s) to be controlled by the programme
b)control measure(s)
c)monitoring procedures that demonstrate that the operational PRPs are implemented
d)corrections and corrective actions to be taken if monitoring shows that the operational PRPs are not in control
e)responsibilities and authorities
f)record(s) of monitoring







