When you receive notification for an International Food Standard audit, it marks the beginning of a critical journey toward certification. This notification isn’t just a formality-it’s your signal to activate a comprehensive preparation plan that can make the difference between certification success and costly delays. Understanding what happens after notification and how to prepare systematically ensures your organization demonstrates compliance while building a stronger food safety culture.

Table of Contents

What is IFS audit notification?

Audit notification is the formal communication you receive from your certification body informing you of an upcoming IFS assessment. The notification period varies depending on the type of audit scheduled. For announced initial audits, you typically receive notification several weeks in advance, providing adequate time to prepare your documentation and team. Surveillance audits may have shorter notification periods, while unannounced audits arrive without prior warning to assess your everyday operations under normal conditions.

Upon receiving notification, your first step should be reviewing the latest IFS standards. The current version is IFS Food Version 8, which became mandatory for all audits starting January 2024. This standard emphasizes food safety culture, risk management, and continuous improvement more strongly than previous versions. Familiarizing yourself with these updated requirements ensures your preparation efforts align with what auditors will assess.

Understanding different types of IFS audits

The type of audit you’re facing determines your preparation approach. Each audit type serves a distinct purpose in the certification process.

Initial audits and their scope

An initial audit represents your first comprehensive evaluation for IFS certification. This thorough assessment covers all aspects of your food safety management system against IFS requirements. Initial audits evaluate quality management systems, HACCP documentation, production processes, and facility conditions. Auditors will spend considerable time reviewing your HACCP plans, standard operating procedures, and quality management records during this phase.

During the document review phase, auditors examine whether your systems are properly designed, documented, and integrated into daily operations. They assess your hazard analysis, critical control points, and monitoring procedures. The site assessment follows, where auditors physically inspect your facility to verify that documented procedures match actual practices on the production floor.

Follow-up audits for corrective actions

Follow-up audits become necessary when significant non-conformities are identified during previous assessments. These focused evaluations specifically examine the corrective actions you’ve implemented to address identified issues. Unlike initial audits that cover your entire system, follow-up audits concentrate on the specific areas where deficiencies were found.

The timeframe for submitting corrective action plans is strict. You must develop and implement corrective actions, then submit evidence to your certification body within four weeks of receiving the audit report. This evidence should demonstrate not just that you’ve fixed the immediate problem, but that you’ve addressed the root cause to prevent recurrence. Missing this deadline can result in requiring a complete re-audit, significantly delaying your certification.

Surveillance audits for ongoing compliance

Surveillance audits are periodic assessments conducted after certification to verify ongoing compliance and monitor improvements. These audits ensure your organization maintains the standards that earned initial certification. The frequency and scope of surveillance audits depend on your previous audit results and overall performance level.

Organizations with higher compliance scores may qualify for less frequent surveillance audits, though maintaining consistent compliance between audits remains crucial for certification continuity. Surveillance audits typically focus on key processes, previous findings, and the effectiveness of your corrective actions since the last assessment.

Conducting a pre-audit assessment

Many organizations conduct internal pre-audits before the official IFS assessment. This practice offers numerous benefits for preparation and confidence building. A pre-audit serves as a rehearsal that helps identify gaps in your systems before external auditors arrive.

During your pre-audit, examine the same areas external auditors will review. Check your documentation for completeness and accuracy. Verify that monitoring records are current and properly maintained. Assess whether your staff can clearly explain their roles in food safety. Walk through your facility with a critical eye, looking for maintenance issues, hygiene concerns, or process deviations that could raise red flags during the official audit.

Pre-audits can be conducted by internal teams with IFS expertise or by external consultants specializing in food safety management systems. The investment in a thorough pre-audit often pays dividends by preventing non-conformities during the actual certification audit.

Essential documentation review

Documentation forms the foundation of your food safety management system. For initial audits, organizing your quality management and HACCP documentation is particularly crucial.

Quality management system documentation

Your quality manual must align with IFS requirements and address all relevant aspects of food safety management. This document should clearly outline your organization’s commitment to food safety, your quality policy, and how your management system operates. Standard operating procedures need to provide clear, detailed instructions for consistent operations across all shifts and personnel.

Document control systems must demonstrate proper management of all quality and food safety documents. Auditors will verify that you have processes for document approval, distribution, revision, and obsolete document control. Records should show that your documented systems are actually implemented, not just theoretical frameworks sitting on a shelf.

HACCP plan and supporting documents

HACCP system documentation must include comprehensive hazard analysis and critical control points that adequately identify, evaluate, and control food safety hazards. Your HACCP plan should include detailed product descriptions, process flow diagrams, hazard analysis worksheets, critical control point determination, critical limits, monitoring procedures, corrective actions, and verification activities.

Process flow diagrams must accurately represent your production sequences and be verified on-site. These visual representations help auditors understand your operations quickly. Supporting documents should include validation studies for critical limits, monitoring records showing your controls are working, and verification records demonstrating periodic evaluation of your HACCP system’s effectiveness.

Preparing your team

While documentation and systems are critical, the human element plays an equally important role in audit success. Your staff must be prepared to effectively demonstrate compliance during the assessment.

All personnel, especially those in key roles, should receive appropriate training on IFS requirements and audit procedures. Training should cover general understanding of the standard’s expectations, familiarity with audit techniques, role-specific responsibilities for food safety, proper record-keeping and document control, and communication protocols for interacting with auditors.

Training should be documented and its effectiveness verified through knowledge assessments or practical demonstrations. Conducting mock audits and interview sessions helps staff become comfortable with the audit process and improves their ability to articulate food safety practices under pressure.

Resource allocation for audit preparation

Successful audit preparation requires adequate resource allocation across multiple areas. This includes personnel time dedicated to preparation activities, budget for necessary improvements or consultations, materials needed for facility or documentation upgrades, external expertise from consultants if needed, and technology tools for document management or verification activities.

Adequate resource allocation demonstrates your organization’s commitment to food safety and increases the likelihood of certification success. This investment in preparation often proves far less costly than dealing with non-conformities or failed audits.

Creating a structured action plan

Following audit notification, develop a detailed action plan that systematically addresses all preparation requirements. Your plan should identify specific tasks, assign clear responsibilities, establish realistic deadlines, allocate necessary resources, and define verification methods to ensure completion.

Break down large preparation tasks into manageable steps. For example, rather than simply listing “update HACCP documentation,” specify individual tasks like reviewing hazard analysis, validating critical limits, updating monitoring forms, and training staff on revised procedures. This granular approach ensures nothing falls through the cracks during the busy preparation period.

What do you think? How effectively does your current preparation process address the comprehensive requirements of IFS certification? What systems could you implement today to ensure your organization maintains audit-ready status continuously rather than scrambling when notification arrives?

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References
  1. https://www.ifs-certification.com/images/ifs_documents/IFS_Food_v8_standard_EN.pdf
  2. https://goaudits.com/blog/ifs-food-version-8/
  3. https://goaudits.com/blog/ifs-audits/
  4. https://auditboard.com/blog/iso-surveillance-audits
  5. https://www.dnv.com/services/ifs-food-standard-5172/
  6. https://safetyculture.com/checklists/ifs-audit/

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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