
Best Answer Tony-C, Yesterday, 05:22 AM
Hi suhaibalbadawi97,
You will need to obtain a copy of all the relevant standards to go through this process. You need to establish the prescribed Prerequisite Programmes in the first place before you can move on to hazard analysis as explained below.
To clarify from ISO 22000 Terms & Definitions food safety hazards include allergens:
3.22 food safety hazard
biological, chemical or physical agent in food (3.18) with the potential to cause an adverse health effect
Note 2 to entry: Food safety hazards include allergens and radiological substances.
With regards to compliance with ISO 22000, in the first place you need to comply with PRP requirements:
ISO 22000 8.2 Prerequisite programmes (PRPs)
8.2.1 The organization shall establish, implement, maintain and update PRP(s) to facilitate the prevention and/or reduction of contaminants (including food safety hazards) in the products, product processing and working environment.
8.2.3 When selecting and/or establishing PRP(s), the organization shall ensure that applicable statutory, regulatory and mutually agreed customer requirements are identified. The organization should consider:
a) the applicable part of the ISO/TS 22002 series;
b) applicable standards, codes of practice and guidelines.
8.2.4 When establishing PRP(s) the organization shall consider:
List a) construction …. to l) others, as appropriate
8.5.1.5.3 Description of processes and process environment
….
c) existing PRPs, process parameters, control measures (if any) and/or the strictness with which they are applied, or procedures that can influence food safety;
You then move on to hazard analysis whilst considering the effectiveness of the prescribed PRPs which I have quoted below.
ISO 22002-100:2025 is intended to be used when establishing, implementing and maintaining the PRPs specific to the organization(s) in conjunction with ISO 22000:2018, 8.2.
ISO 22002-100:2025 Part 100: Prerequisite programmes on food safety —Requirements for the food, feed and packaging supply chain Section 12 Measures for prevention of contamination:
Systems shall be in place to detect, prevent, control or minimize contamination and cross-contamination, to an acceptable level relevant to food safety hazard assessment. Contaminants can include allergens, physical, chemical or biological agents.
NOTE Contamination prevention activities can be highly sector specific. In recognition of this, the different sectors have identified key aspects which are applicable to their specific activities. These can be found in the sector- specific parts of the ISO 22002 series.
For Specific PRPS for Warehouse we refer to ISO 22002-5:2025 Prerequisite programmes on food safety — Part 5: Transport and storage
Allergen Control is NOT in the requirements of ISO 22002-5:2025 so you will need to determine what risks there are in the warehouse operation typical examples include control of open products and control of spillages.
For Specific PRPS for Catering we refer to ISO 22002-2:2025 Prerequisite programmes on food safety — Part 2: Catering Section 12 Measures for prevention of contamination
12.2 Allergen Control. Here there are extra specified requirements:
Products shall be protected from unintended allergen cross-contact, as applicable, by:
a) cleaning;
b) segregation;
c) additional protective clothing;
d) use of dedicated tools/equipment.
NOTE Allergen cross-contact can arise from either:
……
There are other requirements to make relevant allergen information available to the consumer, address allergen control in meal preparations and specific training in allergen awareness.
For those working with FSSC 22000, FSSC 22000 Version 6 Additional Requirements apply:
2.5.6 MANAGEMENT OF ALLERGENS (ALL FOOD CHAIN CATEGORIES)
The organization shall have a documented allergen management plan that includes:
a) A list of all the allergens handled on site, including in raw materials and finished products;
b) Risk assessment covering all potential sources of allergen cross-contamination;
c) Identification and implementation of control measures to reduce or eliminate the risk of
cross-contamination, based on the outcome of the risk assessment; and
d) Validation and verification of these control measures shall be implemented and maintained as documented information. ………………
Note there are further requirements e) to h)
Kind regards,
Tony
