HACCP records sheet -

HACCP records sheet

HACCP stand for Hazard analysis and critical control points

Hazard analysis and its controlling for the foods products, health care products, medicines etc. product that directly concern with human health that required much awareness of the hazards and required fully controls on critical things and material which is harm human health, HACCP record sheet is one of the most important document for the manufacturing and processing companies that food and medicines producers are mostly used for the controls. Here as below given example format for HACCP records sheet:

HACCP numbers – Number should be unique and easier for traceability.
Steps or process name – each process, activities are needs to mention for understanding of controls and its requirements.
Identification of hazard in process, step that is concern with manufacturing activities and sub activities.
Control measure – Control measures also needs to define for the each activity, sub activities.
Critical limit – What is critical limits for each process and steps
Monitoring – manufacturing process required monitoring to find out hazards, identification of controls and deployments, monitoring help to stage wise activities and its critical requirements identification to enable action planning.
Correction – during the monitoring, in each process, stages, controls and to consider its criticality what correction required to perform better and eliminate hazards of the process.
Corrective action – on base of the correction, what should be requirements for elimination, process change or other concern modifications are required to enable controlling on process and its sequences to eliminate hazard’s possibility

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HACCP records sheet

HACCP stand for Hazard analysis and critical control points

HACCP numbers – Number should be unique and easier for traceability.

Steps or process name – each process, activities are needs to mention for understanding of controls and its requirements.

Identification of hazard in process, step that is concern with manufacturing activities and sub activities.

Control measure – Control measures also needs to define for the each activity, sub activities.

Critical limit – What is critical limits for each process and steps

Monitoring – manufacturing process required monitoring to find out hazards, identification of controls and deployments, monitoring help to stage wise activities and its critical requirements identification to enable action planning.

Correction – during the monitoring, in each process, stages, controls and to consider its criticality what correction required to perform better and eliminate hazards of the process.

Corrective action – on base of the correction, what should be requirements for elimination, process change or other concern modifications are required to enable controlling on process and its sequences to eliminate hazard’s possibility

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