7 Principles of HACCP Certification – Food Safety Management Systems

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  • The likely occurrence of hazards and severity/consequence of their adverse health effects or effect on product quality or regulatory compliance
  • Qualitative and/or quantitative evaluation of the presence of hazards
  • Survival or multiplication of micro-organisms
  • Production, persistence or cross-contamination of toxins, chemicals or physical agents


  • Established food safety principles or published research
  • Legislative requirements

  • Responsibility – job title of the individual who will carry out the monitoring
  • Frequency – if not continuous then at a frequency sufficient to ensure that the CCP is under control.
  • Method – detailed specification or procedure
  • Records to be kept – including action limits and critical limits, the results of monitoring activity, the signature of the responsible person and verification countersignature.

  • Immediate action to re-establish control before the deviation leads to a CCP breach
  • Responsibility for the corrective action
  • Immediate action to re-establish control
  • Identification of all product produced since the critical limit was breached (since last in control monitoring result)
  • Disposition of affected product
  • Responsibility for the corrective action

  • Microbiological and chemical testing (where applicable) to confirm CCPs, QCPs and RCPs are in control. The schedule includes the type and frequency of testing which has been determined by the risk nature of the products and processes and covers all finished products.
  • Shelf-life validations covering both microbiological and sensory testing (where applicable). The schedule includes the type and frequency of testing.
  • Physical assessments of products against specifications. Methods for assessment, responsibilities and frequency of assessment are defined.
  • Reviewing internal incidents, non-conforming product records, customer complaints, withdrawals or recalls relating to food safety, quality or legality.
  • Internal audits of CCP monitoring and corrective action records

  • The HACCP Plan, Objectives, Scope, Regulatory & Customer Requirements
  • HACCP Development Team Meeting Minutes
  • Finished Product Descriptions
  • Process Flow Diagrams
  • Hazard Analysis
  • CCP Determination and Validation
  • Critical Limit / Action Limit Determination
  • CCP Monitoring Procedures and Corrective Action Procedures
  • CCP Monitoring Records
  • Corrective Action Records
  • HACCP Training records and competency assessments for operators, supervisors and managers
  • Evidence of HACCP management including:
    • Verification Schedule and Records
    • Team Meeting Minutes
    • Modification records

 

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  • The likely occurrence of hazards and severity/consequence of their adverse health effects or effect on product quality or regulatory compliance
  • Qualitative and/or quantitative evaluation of the presence of hazards
  • Survival or multiplication of micro-organisms
  • Production, persistence or cross-contamination of toxins, chemicals or physical agents


  • Established food safety principles or published research
  • Legislative requirements

  • Responsibility – job title of the individual who will carry out the monitoring
  • Frequency – if not continuous then at a frequency sufficient to ensure that the CCP is under control.
  • Method – detailed specification or procedure
  • Records to be kept – including action limits and critical limits, the results of monitoring activity, the signature of the responsible person and verification countersignature.

  • Immediate action to re-establish control before the deviation leads to a CCP breach
  • Responsibility for the corrective action
  • Immediate action to re-establish control
  • Identification of all product produced since the critical limit was breached (since last in control monitoring result)
  • Disposition of affected product
  • Responsibility for the corrective action

  • Microbiological and chemical testing (where applicable) to confirm CCPs, QCPs and RCPs are in control. The schedule includes the type and frequency of testing which has been determined by the risk nature of the products and processes and covers all finished products.
  • Shelf-life validations covering both microbiological and sensory testing (where applicable). The schedule includes the type and frequency of testing.
  • Physical assessments of products against specifications. Methods for assessment, responsibilities and frequency of assessment are defined.
  • Reviewing internal incidents, non-conforming product records, customer complaints, withdrawals or recalls relating to food safety, quality or legality.
  • Internal audits of CCP monitoring and corrective action records

  • The HACCP Plan, Objectives, Scope, Regulatory & Customer Requirements
  • HACCP Development Team Meeting Minutes
  • Finished Product Descriptions
  • Process Flow Diagrams
  • Hazard Analysis
  • CCP Determination and Validation
  • Critical Limit / Action Limit Determination
  • CCP Monitoring Procedures and Corrective Action Procedures
  • CCP Monitoring Records
  • Corrective Action Records
  • HACCP Training records and competency assessments for operators, supervisors and managers
  • Evidence of HACCP management including:
    • Verification Schedule and Records
    • Team Meeting Minutes
    • Modification records

 

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