TÜV NORD CERT BRC Standard for Food Safety, Version 7

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Fact Sheet TÜV NORD CERT BRC Standard for Food Safety, Version 7 TÜV NORD CERT GmbH Tel. : +49 (0) 511 9986-1222 Fax: +49 (0) 511 9986-69 1900 info.tncert@tuev-nord.de The BRC Global Standard for food safety was developed in order to specify in more detail the safety, quality and operational criteria for fulfilment of the applicable legal regulations and consumer protection measures in the food industry. The certification is recognised by many food retailers, food service companies and manufacturers worldwide in their assessment of the capabilities of their suppliers. Target groups The BRC standards are intended for food manufacturers in particular those producing private labels, but also brand manufacturers, suppliers etc. and also for manufacturers of packaging and packaging materials for the food industry and other sectors. BRC certification is of particular interest to companies who export to Great Britain. Scope The BRC specifies requirements for the manufacture of processed foods and preparation of primary products which are supplied as private labels of a particular retailer and branded foods and food or ingredients for use by catering companies, restaurants and food manufacturers. Important changes in BRC Food Version 7 As of 1 July 2015, the seventh version of BRC Food will be mandatory and supersede BRC Food 6. The following changes are significant: 1. New fundamental requirements* The ten fundamental requirements from Version 6 are retained, and there are two new fundamental requirements regarding label control and supplier management. 2. Changed scoring system from now on, grades AA, A, B, C and D will be assigned. 3. Free selection of unannounced programmes* now applies to all sites. 4. New BRC Programme Global Markets * 5. Additional voluntary modules* can be included in the audit. 6. Traceability the requirement for traceability becomes stricter, particularly in relation to suppliers. 7. Authenticity in order to estimate the probability of counterfeits and prevent food fraud, risk assessments must be carried out and any necessary measures taken and/or sampling procedures introduced. 8. Extended zone concept In addition to the high care and high risk zones for products with mandatory refrigeration, from now on there will also be a risk class for non-refrigerated products with high-care requirements. In addition, all operating areas must be divided into zones, which must be represented as plans. * Further information is available in this Fact Sheet 1

The certification only applies for products which are manufactured or prepared at the audited site, and includes storage facilities which are under the direct control of the production site management. The standard does not apply for: Food products which are not further processed at the audited site, or Activities associated with wholesale, importation, delivery or storage outside the direct control of the company. Benefits Many retailers and food manufacturers only approve suppliers with BRC certification Supply capability is evidenced by means of listing and registration in the BRC database drawing attention to certified suppliers Enhanced image of certified companies Reduction of risks and warranty claims Possibility of efficient and cost-effective combined audits (e.g. linked with other management systems/food safety systems) Product categories Audit scope Individual categories 1 Raw red meat Raw products of animal or vegetable origin that require cooking prior to consumption 2Raw poultry 3 Raw prepared products (meat and vegetarian) 4 Raw fish products and preparations Fruit, vegetables and nuts Processed foods and liquids with pasteurisation with UHT as heat treatment or similar technology 5 Fruit, vegetables and nuts 6 Prepared fruit, vegetables and nuts 7 Dairy, liquid egg 8 Cooked meat/fish products Processed foods, ready to eat or heat 9 Raw cured and/or fermented meat and fish 10 Ready meals and sandwiches, ready-to-eat desserts Ambient stable products with pasteurisation or sterilisation as heat treatment 11 Low/high acidic products in cans/glass 12 Beverages 13 Alcoholic drinks and fermented/brewed products Ambient stable products not involving sterilisation as heat treatment 14 Bakery 15 Dried food and ingredients 16 Confectionery 17 Cereals and snacks 18 Oils and fats 2

Preconditions In addition to fulfilment of the requirements of the standard, the following criteria are decisive for certification according to BRC: Application of the principles of Hazard Analysis and Critical Control Point (HACCP) and Good Manufacturing Practice (GMP) Analysis of processes/technologies in the manufacturing of products and/or packaging Fulfilment of legal regulations with regard to facilities and equipment, products and services as well as qualification of personnel Classification of risks Auditing of the quality management system Certification procedure Offer by TÜV NORD CERT based on information provided Order for certification Audit planning Certification audit Nonconformity management (if appropriate) Release of the certification process by the certification body Award of certificate (depending on result, between 6 and 12 months) and registration in the BRC database Audit duration The duration of the audit depends on the following factors: Number of employees (calculated on the basis of the full-time employees, including seasonal work) Size of the production facility (including storage areas) Number of HACCP studies (One HACCP study relates to product groups with similar risks and manufacturing methods/technologies) 50 per cent of the calculated time is assigned to assessment of production. The company must ensure that the manufacturing processes for the products included in the scope of the certificate can be assessed during the audit. Audit options a) Announced The audit date is agreed with TNC before the audit, and all requirements of the standard are assessed during the audit itself. Successful sites receive a certificate with grade AA, A, B, C or D, depending on the number and severity of nonconformities identified. b) Unannounced Unannounced audits offer sites the opportunity to demonstrate the maturity of their quality systems. Depending on the nonconformities identified during the audit, the grades AA+, A+, B+, C+ or D+ are awarded. There are two options for unannounced audits. In the case of Option 1, fulfilment of the entire standard is assessed during one single unannounced audit (~2-3 days). With Option 2, the audit visit is divided into two separate areas (with ~1-2 days each). During the first, unannounced visit good manufacturing practices will primarily be assessed, whilst the second, announced part concentrates on documented systems and documentary evidence. c) Global markets This three-stage programme corresponds to the GFSI Global Markets Programme and is most suitable for companies who are new to the standard and in the process of developing their food safety system. The programme allows sites to be assessed according to specified requirements of the BRC, which are categorised as basic or intermediate food safety requirements. This means that sites receive recognition at a basic or intermediate level before they finally achieve complete certification. 3

Voluntary modules The standard has been designed to allow the addition of voluntary modules to the routine audit. The voluntary modules mean that sites can demonstrate compliance with specific groups of requirements in order to fulfil certain market or customer conditions. Every audit option can be added to the complete certification. A list of voluntary modules, the applicable requirements and all specific clauses relating to them is available on the BRC website (www.brcglobalstandards.com). Requirements The current requirements for certification to BRC 7 are assigned to seven main clauses. Within the standard, certain requirements are described as fundamental. These are shown in the diagram below in addition to the main clauses. Non-fulfilment of a fundamental requirement (i.e. a significant nonconformity) leads to non-certification in an initial audit or withdrawal of the certification if the nonconformity is identified in subsequent audits. If this occurs, a further full audit is necessary in order to provide evidence of fulfilment. 6.1: Control of operations Senior management commitment 1.1: Senior management commitment and continual improvement 6.2: Labelling and pack control Personnel Food safety plan HACCP 2: HACCP Plan Food safety and quality 7.1: Training: Raw material handling, preparation, processing, packing and storage areas Process control Product control Food safety and quality management system Site standards 3.4: Internal audits 3.5.1: Management of suppliers of raw materials and packaging 5.3: Management of allergens 4.3: Layout, product flow and segregation 3.7: Corrective and preventive actions 3.9: Traceability 4.11: Housekeeping and training 4

Nonconformities There are three grades of nonconformities: Critical: Where there is a critical failure to comply with a food safety or legal issue Major: Where there is a critical failure to meet the requirements of a statement of intent or any clause of the Standard or a situation is identified which would, on the basis of available objective evidence, raise significant doubt as to the conformity of the product being supplied Minor: Where a clause has not fully been met but, on the basis of objective evidence, the conformity of the product is not in doubt. Audits can cover several sites with different addresses if: all sites are under the same organisation ownership, all sites are operated with the same documented quality management system, the sites manufacture products that are a part of the same manufacturing process, the sites only supply the other sites, with no additional customers, and the sites are not more than 50 kilometres (30 miles) apart. Further information Further information as well as the Standard itself are available at the BRC website for downloading: www.brcglobalstandards.com/ If nonconformities are identified, the company must present the auditor with an action plan within 28 days along with evidences that prove that the nonconformities have been corrected or that corrections have been instigated (e.g. in case of actions concerning buildings). Audits covering several sites Generally, the audit, the report and the certificate are product- and site-specific. Under some circumstances, however, more than one site can be included in one certification. If you have any further questions, please contact TÜV NORD CERT directly. TÜV NORD CERT GmbH Tel. : +49 (0) 511 9986-1222 Fax: +49 (0) 511 9986 69-1900 info.tncert@tuev-nord.de www.tuev-nord-cert.com 24-0302-07/15 5