After months of preparation and a rigorous audit, food manufacturers await the moment when their efforts culminate in receiving an IFS certificate. But what happens between the final audit day and holding that certificate in hand? The process of awarding an IFS certificate involves multiple carefully orchestrated steps that ensure only facilities meeting stringent food safety and quality standards receive certification.

Table of Contents

Understanding the role of certification bodies

The certification body plays a central role in awarding IFS certificates. These organizations must be accredited according to ISO/IEC 17065:2012 standards and maintain a valid contract with IFS Management GmbH. They serve as independent third-party assessors who evaluate whether a company meets all requirements of the IFS standard.

Once the on-site audit concludes, the certification body assumes responsibility for making the final certification decision. This decision cannot be made lightly or immediately. The auditor provides only a provisional assessment during the closing meeting, as the formal certification process requires thorough review of documentation, corrective action plans, and evidence of compliance.

The timeline from audit to certificate

The journey from completed audit to certificate issuance follows a strict timeline designed to balance thoroughness with efficiency. The standard timeline spans six to eight weeks, broken into distinct phases that ensure proper verification of compliance.

Pre-report preparation

Within two weeks of the audit date, the auditor prepares a preliminary report outlining all findings from the assessment. This pre-report documents any deviations or non-conformities discovered during the audit, along with observations about the company’s food safety management systems. The preliminary nature of this document allows the company to understand areas requiring attention before the final certification decision.

Corrective action plan submission

Companies then have four weeks to respond to identified deviations and non-conformities by developing a comprehensive corrective action plan. This plan must detail both immediate corrections and long-term corrective actions addressing root causes of problems. Missing this four-week deadline can result in the need for a complete re-audit, potentially delaying certification for months.

The corrective action plan requires more than simply stating intentions. Companies must provide evidence that corrections have been implemented, along with detailed descriptions of preventive measures to ensure issues do not recur. The plan should address each finding systematically, demonstrating a commitment to continuous improvement in food safety practices.

Review and approval

The final two weeks involve the auditor and certification body reviewing the submitted action plan. During this critical phase, they verify that all corrections have been properly implemented and that proposed corrective actions are adequate. If the certification body finds the corrective actions invalid, inadequate, or irrelevant, they return the action plan to the company for completion within the established timeframe.

This review process also includes preparing the final audit report and uploading documentation to the IFS Database. The certification body’s technical committee examines all evidence collected by auditors and the information from the entire process before making their final determination.

Certificate validity and the audit cycle

Once awarded, an IFS certificate remains valid for one year from the date of issue stated on the certificate. This annual certification cycle ensures that certified companies maintain their food safety and quality standards consistently rather than allowing systems to deteriorate between longer intervals.

The renewal audit date is calculated from the date of the initial audit, not from the certificate issue date. This distinction matters significantly for scheduling purposes. Companies receive reminders from the IFS Database three months before their certificate expiration, allowing adequate time to schedule and prepare for recertification.

The audit cycle operates on a three-year framework requiring annual audits to maintain certification. Every third audit must be unannounced, demonstrating that the company maintains high food safety standards even without advance preparation. This unannounced audit approach provides retailers and other stakeholders confidence that certified suppliers consistently meet requirements.

Critical requirements for certificate issuance

Not all audit results lead to certification. The IFS standard establishes specific criteria that companies must meet before receiving a certificate. Understanding these requirements helps organizations focus their improvement efforts where they matter most.

Major non-conformities

The standard’s regulation does not allow certificate issuance when more than one Major non-conformity exists. This strict rule reflects the critical importance of certain food safety requirements. Major non-conformities indicate significant failures in systems protecting food safety, and multiple such failures suggest systemic problems requiring resolution before certification.

When auditors identify Major non-conformities during an audit, companies must undergo a follow-up audit within six months. This follow-up focuses specifically on verifying that actions taken have effectively corrected the Major non-conformity. For production-related failures, the follow-up audit must occur at least six weeks after the previous audit but no later than six months afterward.

Knock-out requirements

The IFS standard identifies ten requirements as extremely critical, designated as Knock-Out requirements. These include governance and commitment, monitoring systems for critical control points, personal hygiene, raw material specifications, product compliance, foreign material risk mitigation, traceability, internal audits, withdrawal and recall procedures, and corrective actions. Failure in any Knock-Out requirement results in automatic denial of certification, regardless of performance in other areas.

The scoring system and certification levels

IFS employs a quantified assessment system that expresses compliance as a percentage. This scoring approach allows both certification bodies and the company’s customers to evaluate performance objectively. The standard recognizes two certification levels based on these scores.

Higher Level certification requires achieving a score above 95 percent, indicating exceptional compliance with minimal deviations. Foundation Level certification applies to scores between 75 and 95 percent, demonstrating that the company meets basic requirements while having room for improvement. Scores below 75 percent or failure in any Knock-Out requirement mean no certification is granted.

Database upload and certificate distribution

Once the certification body makes a positive certification decision, they upload the audit report, approved corrective action plan, and certificate to the IFS Database. This centralized database serves as the authoritative source for verifying certificate validity and authenticity. Retailers and other stakeholders can access this information to confirm their suppliers’ certification status.

The company receives its certification package via email, including the certificate, final audit report, and approved corrective action plan. This documentation provides evidence of compliance that companies can share with customers and use for internal quality improvement initiatives. The certification body stores this evidence for three years, ensuring accessibility for future reference or audits.

Maintaining certification over time

Receiving an IFS certificate represents an achievement, but maintaining it requires ongoing commitment. The annual recertification audit assesses whether the company continues meeting standards and has implemented improvements from previous audits. Particular attention focuses on the effectiveness of corrective actions from earlier assessments, even if that previous audit occurred more than one year ago.

Companies must inform their certification body if they have been IFS certified in the past, regardless of which certification body conducted previous audits. This requirement ensures continuity in the assessment process and allows auditors to verify that previous non-conformities have been adequately addressed through sustained corrective actions.

If companies fail to perform their renewal audit within the specified timeframe, the IFS Database automatically notifies all users who have added that production site to their favorites list. This transparency helps retailers and other stakeholders make informed decisions about their supply chain partners based on current certification status.

What do you think? How can food manufacturers best prepare for the certificate awarding process? What strategies help ensure corrective action plans effectively address audit findings?

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References
  1. https://www.ifs-certification.com/en/
  2. https://en.eurocert.group/certifications/ifs-food
  3. https://goaudits.com/blog/ifs-audits/
  4. https://www.asifood.com/asi-food-safety-blog/international-featured-standards-certification-what-you-need-to-know-about-ifs
  5. https://www.ifs-certification.com/images/ifs_documents/IFS_Food_v8_standard_EN_1711635033.pdf

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Food Safety and Quality Management Systems

1 Introduction to Management systems

  1. Introduction to ISO 9001
  2. ISO 9000
  3. Introduction to ISO 14001:2004
  4. How to Use ISO 14001
  5. Introduction to OHSAS 18001:2007
  6. How to Use OHSAS 18001:2007
  7. Introduction to ISO/IEC 27001
  8. The PDCA Model

2 Auditing

  1. Clause 1 – Scope of the Standard
  2. Clause 2 – Normative References
  3. Clause 3 – Terms and Definitions
  4. Clause 4 – Principles of Auditing
  5. Clause 5 – Managing an Audit Program
  6. Clause 6 – Audit Activities
  7. Clause 7 – Competence and Evaluation of Auditors

3 Standardization and Accreditation

  1. International Accreditation Forum (IAF)
  2. International Laboratory Accreditation Cooperation (ILAC)
  3. Quality Council of India (QCI)
  4. National Accreditation Board for Testing and Calibration Laboratories (NABL)
  5. ISO/TS 22003:2007 Food Safety Management System
  6. ISO Guide 65: General Requirements for Bodies Operating Product Certification Systems
  7. ISO/IEC 17020:1998 General Criteria for the Operation of Various Types of Bodies Performing Inspections
  8. ISO/IEC 17021:2006 – Conformity Assessment-Requirements for Bodies Providing Audit and Certification of Management Systems
  9. ISO 17025:2005 General Requirements for the Competence of Testing and Calibration Laboratories

4 ISO 9001-2000 – An Overview

  1. ISO 9000
  2. Quality Management Principles
  3. ISO 9000:2005, Quality Management Systems: Fundamentals and Vocabulary
  4. ISO 9001:2000, Quality Management Systems: Requirements
  5. Steps for Implementing Quality Management Systems
  6. Benefits of ISO 9001:2000
  7. ISO 9004:2000, Quality Management Systems: Guidelines for Performance Improvements
  8. Relationship with ISO 9001:2000
  9. Self-assessment Model

5 ISO 9001-2000 – Structure

  1. Documentation Structure of ISO 9001:2000
  2. Quality Manual
  3. Mandatory Procedures
  4. Standard Operating Procedures (SOPs)
  5. Process Definition Documents
  6. Work Instructions
  7. Miscellaneous Documents
  8. Formats and Records
  9. ISO 9001:2000 Clauses

6 Clause wise interpretation of ISO 9001-2000

  1. Clause 1: Scope
  2. Clause 2: Normative Reference
  3. Clause 3: Terms and Definitions
  4. Clause 4: Quality Management System
  5. Clause 5: Management Responsibility
  6. Clause 6: Resource Management
  7. Clause 7: Product Realization
  8. Clause 8: Measurement, Analysis and Improvement

7 ISO 9001-2000 – Case Studies

  1. Engineering Job Work Organisation
  2. Software Development Organisation
  3. Management Review in Engineering
  4. Customer-Related Processes in Software
  5. Internal Audits in Engineering
  6. Design and Development in Software
  7. Corrective and Preventive Actions in Software
  8. Customer Property Management in Engineering

8 ISO 22000-2005 – An Overview

  1. What Does ISO 22000 Bring to the HACCP Method?
  2. System Components
  3. Communication between Participants in the Food Industry
  4. ISO 22000: A Passport for Exporting?
  5. Why do Companies Commit themselves to an ISO 22000 Approach?
  6. Who Should Use ISO 22000:2005?
  7. Why Use ISO 22000:2005?
  8. ISO 22000 and HACCP
  9. Codex Alimentarius
  10. Key Elements and Benefits of ISO 22000

9 ISO 22000-2005 – Structure

  1. Economic Loss due to Food Borne Illness
  2. ISO 22000: 2005 Clauses
  3. FSMS Documentation Structure
  4. Food Safety Team Structure
  5. Food Safety Manual
  6. Mandatory Procedures
  7. Standard Operating Procedures (SOP)/Work Instructions
  8. HACCP Pre-steps Related Documents
  9. HACCP Principles Related Documents
  10. Miscellaneous Documents
  11. Formats and Records

10 Clause-wise interpretation of ISO 22000- 2005

  1. Clause 1: Scope
  2. Clause 2: Normative References
  3. Clause 3: Terms and Definitions
  4. Clause 4: Food Safety Management System
  5. Clause 5: Management Responsibility
  6. Clause 6: Resource Management
  7. Clause 7: Planning and Realization of Safe Products
  8. Clause 8: Validation, Verification and Improvement of the FSMS

11 ISO 22000-2005-Case Studies

  1. Kick-off meeting
  2. Introduction to the standard
  3. Formation of food safety team
  4. Description of product and its intended use
  5. PRP (Pre-requisite programme)
  6. Flow diagrams, process steps and control measures
  7. Control measure assessment
  8. Verification of food safety management system
  9. Traceability system
  10. External communication
  11. Internal communication
  12. Management Reviews

12 An Overview and Requirements of ISO 17025

  1. Introduction to the ISO/IEC 17025 Standard
  2. Scope of ISO/IEC 17025
  3. Normative References
  4. Terms and Definitions
  5. General Requirements
  6. Structural Requirements
  7. Resource Requirements
  8. Process Requirements
  9. Management System Requirements

13 Requirements specific to Food testing laboratories – Physical and chemical Parameters

  1. Introduction
  2. Quality and Safety Requirements of Food Products
  3. Chemical and Physical Testing Requirements of Food Products
  4. Laboratory Quality Management System
  5. Management Requirements (Clause 4 of ISO 17025)
  6. Technical Requirements (Clause 5 of ISO 17025)
  7. Traceability of Measurement
  8. Sampling
  9. Handling Test and Calibration Items
  10. Assuring the Quality of Test and Calibration Results

14 Requirements specific to Food testing laboratories – Biological parameters

  1. Introduction
  2. Quality and Safety Requirements of Food Products
  3. Biological Testing Requirements of Food Products

15 General topics- related to Food testing laboratories

  1. Method Validation
  2. Ruggedness
  3. Uncertainty of Measurement
  4. International Accreditation Aspects

16 BRC Food and BRC/IOP Standards – An Overview

  1. BRC Global Standard – Food (Issue 5, January 2005)
  2. Introduction to BRC Food Standard
  3. Legislative Requirements
  4. Benefits of the BRC Global Standard – Food
  5. Principles of the BRC Global Standard – Food
  6. The Standard Technical Advisory Committee
  7. Scope of the BRC Global Standard – Food
  8. The Format of the BRC Global Standard – Food
  9. Application
  10. Structure and Interpretation of the Standard
  11. BRC / IOP Global Standard Issue 3 2001 (Food Packaging and Other Packaging Materials)
  12. IOP: The Institute of Packaging
  13. BRC/IOP Relationship
  14. Benefits of BRC/IOP Packaging Standard
  15. Principles of BRC/IOP Packaging Standard
  16. Application
  17. Structure of BRC / IOP Global Standard – Food Packaging and Other Packaging Materials

17 International Food Standard

  1. Background of the IFS
  2. Service Protocol of the IFS ISSUE 5
  3. Contractual Arrangements – Selection of Certifying Body
  4. Audit Notification
  5. Scope of the Audit
  6. Audit Flow – Preparing the Audit Plan
  7. Level Determination – KO, Major NC’s, NA
  8. Scores, Issuing the Audit Report and Certification
  9. Audit Frequency
  10. Audit Report
  11. Awarding of Certificate
  12. Distribution of the Audit Report
  13. Supplementary Action
  14. Appeal Procedure
  15. Complaints
  16. IFS – Catalogue of Requirements
  17. Management of Quality System
  18. Management Responsibility
  19. Resource Management
  20. Product Realization
  21. Measurements, Analysis and Improvements
  22. Requirements for Certification Bodies and Auditors
  23. Report

18 SQF 1000 And SQF 2000

  1. SQF 1000
  2. Interpretation of SQF 1000 Standard
  3. SQF 2000
  4. Interpretation of SQF 2000 Standard
  5. Let Us Sum Up

19 Global GAP and India GAP

  1. Potential Benefits and Challenges Related to Good Agricultural Practices (GAP)
  2. Description of the FAO/GAPs
  3. USDA GAP/GHP Programme
  4. Global GAP
  5. India GAP