Difference Between ISO 9001 - 2015 Vs ISO 22000 - 2018
Difference Between ISO 9001 - 2015 Vs ISO 22000 - 2018
Difference Between ISO 9001 - 2015 Vs ISO 22000 - 2018
1.0 Scope
2.0 Normative references
3.0 Terms and Definitions
4.0 Context of the Organization
4.1 Understanding the Organization and Its Context
4.2 Understanding the Needs and Expectations of Interested Parties
4.3 Determining the Scope of the Quality/Food Safety Management System
4.4 Quality/ Food Safety Management System and its processes
5.0 Leadership
5.1 Leadership & Commitment
5.1.1 General
5.1.2 Customer focus
5.2 Quality Policy
5.2.1 Establishing the Quality/food safety Policy
5.2.2 Communicating the quality/food safety policy
5.3 Organizational Roles Responsibilities and Authorities
6.0 Planning
6.1 Actions to Address Risks and Opportunities
6.2 Quality/food safety Objectives and Planning to Achieve Them
6.3 Planning of changes
7.0 Support
7.1 Resources
7.1.1 General
7.1.2 People
7.1.3 Environment for the Operation of Processes / infrastructure
7.1.4 Monitoring and Measuring Resources/work environment
7.1.5 Organizational Knowledge/Externally developed elements of the food safety
management system
8.4.1 General
8.4.2 Type & extent of control
8.4.3 information for external providers
8.5 Hazard Control
8.5.1 Preliminary steps to enable hazard analysis
8.5.2 Hazard analysis
8.5.3 Validation of control measure (s) and combination of control measures
8.5.4 Hazard control plan (HACCP/OPRP plan)
8.5 Production and Service Provision
8.5.1 Control of Production and Service Provision
8.5.2 Identification and Traceability
8.5.3 Property Belonging to Customers or External Providers
8.5.4 Preservation
8.5.5 Post-Delivery Activities
8.5.6 Control of Changes
8.6 Release of Products and Services/ Updating the information specifying the PRPs and the
hazard control plan
8.7 Control of Nonconforming Outputs / Control of monitoring and measuring
8.8 Verification related to PRPs and the hazard control plan
8.8.1 Verification
8.8.2 Analysis of results of cerification activities
8.9 Control of product and process nonconformities
8.9.1 General
8.9.2 Corrections
8.9.3 Corrective actions
8.9.4 Handling of potentially unsafe products
8.9.5 Withdrawal / recall
9.0 Performance Evaluation
9.1 Monitoring, Measurement, Analysis and Evaluation
9.1.1 General
9.1.2 Customer Satisfaction