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Registrar Corp Online Training

Registrar Corp Online Training

100% Online, Self-Paced Food Safety Training

  • FOOD SAFETY
    • PCQI
      • HUMAN FOOD
      • ANIMAL FOOD
    • FSVP
    • HACCP
      • CERTIFICATION
      • JUICE HACCP CERTIFICATION
      • FOUNDATIONS OF HACCP
      • HACCP + SQF
      • HACCP + FSSC 22000
      • HACCP + BRCGS
    • SQF
      • PRACTITIONER
      • MASTERING SQF
      • INTERNAL AUDITOR
      • TEMPLATES
      • FOOD SAFETY CULTURE
    • FSSC 22000
      • TEAM LEADER
      • UNDERSTANDING
      • IMPLEMENTING
      • INTERNAL AUDITOR
      • TEMPLATES
      • FOOD SAFETY CULTURE
    • BRCGS
      • TEAM LEADER
      • INTRODUCTION
      • MASTERING
      • INTERNAL AUDITOR
      • TEMPLATES
    • ISO 22000
      • TEAM LEADER
      • INTRODUCTION
      • MASTERING
      • INTERNAL AUDITOR
      • TEMPLATES
    • FDA COURSES
    • BETTER PROCESS CONTROL SCHOOL
      • ACIDIFIED
      • ASEPTIC
      • RETORT
      • ACIDIFIED + RETORT
    • TRAIN PRODUCTION WORKERS
      • Employee Training Package
    • INTERNAL AUDITS
      • SQF
      • FSSC 22000
      • BRCGS
      • ISO 22000
      • ISO 9001
  • COSMETICS
    • MoCRA
    • GMP (ISO 22716)
    • QUALITY TRAINING PACKAGES
    • ISO 9001 for COSMETICS
    • NON-CLINICAL GLP
    • PRESERVATIVE EFFICACY TESTING
  • DRUGS
  • MEDICAL DEVICES
    • ISO 13485
      • INTRODUCTION
      • IMPLEMENTING
    • EU MDR
  • CONTACT

What is a Gap Analysis?

What is a Gap Analysis?

One of the first steps in your Food Safety Management System (FSMS) implementation project is to compare your current FSMS to the requirements of the standard. This is most commonly called a Gap Analysis.

The most important tool for the Gap Analysis is the Audit Checklist. This is a list of the requirements in the code, written in question format. The auditor will use this list to compare your current system with the requirements of the standard.

Scheduling and Performing the Gap Analysis

Schedule the audit ahead of time, so you can inform employees about the Gap Analysis. Allow enough time to do an in-depth audit. The more information you can provide the more efficient and effective your project will be.

When the audit has been completed, meet with the auditors to summarize the results. These results will be transferred to task lists for the implementation. This meeting should be held shortly after the audit, so that information is fresh in the auditors’ memory.

A. Scheduling the Gap

Review the project plan:

  • Who did you identify to conduct the gap?
  • Schedule the Gap Analysis, and communicate to all employees what is being done, and why. You will want to be able to make the employees comfortable with answering your auditor’s questions.
  • You may want to consider sending out a newsletter to inform employees that the Gap will be performed, by whom, when and why the Gap is being performed.

The audit schedule

  • Determine if you will audit by process/procedure or by area of the facility. Our approach is usually to audit by area of the facility.
  • Divide the facility into manageable areas.
  • Schedule time to audit each section of the standard that applies to the area.
  • If you are using an audit team, assign the team to cover the various areas of the facility.
  • Arrange your Gap Analysis checklists so each auditor will have the sections of the standard that are applicable in the areas they will cover.
  • Arrange your checklists so each auditor will have the sections of the standard that are applicable in the areas they will cover.

B. Conducting the Audit

Follow the schedule that you have prepared. Go into each area of the facility to evaluate the current quality system.

  • Focus on what is in place, and what is not in place. Remind auditors that you are not focusing on compliance or non compliance to the current system, but on the design of the current system, and how it matches the FSSC requirements.
  • Take notes on what is in place, and what will need to be developed and changed. Take complete notes, reference documents and examples.

C. Reporting

Summarize the audit findings in the form of a task list. You will usually identify several categories of tasks.

  • Processes that comply with the standard and are documented.
  • Processes that comply with the standard and must be documented.
  • Processes that do not comply with the standard and must be redesigned.
  • Processes required by the standard that are not currently in place.
  • For each requirement (or set of requirements) of the standard you will want to identify the status of the current system. The Steering Team will use this information as they assign responsibility and timelines to Teams. Task Teams will be assigned responsibility for development of a procedure.

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  • FOOD SAFETY
    • PCQI
      • HUMAN FOOD
      • ANIMAL FOOD
      • Back
    • FSVP
    • HACCP
      • CERTIFICATION
      • JUICE HACCP CERTIFICATION
      • FOUNDATIONS OF HACCP
      • HACCP + SQF
      • HACCP + FSSC 22000
      • HACCP + BRCGS
      • Back
    • SQF
      • PRACTITIONER
      • MASTERING SQF
      • INTERNAL AUDITOR
      • TEMPLATES
      • FOOD SAFETY CULTURE
      • Back
    • FSSC 22000
      • TEAM LEADER
      • UNDERSTANDING
      • IMPLEMENTING
      • INTERNAL AUDITOR
      • TEMPLATES
      • FOOD SAFETY CULTURE
      • Back
    • BRCGS
      • TEAM LEADER
      • INTRODUCTION
      • MASTERING
      • INTERNAL AUDITOR
      • TEMPLATES
      • Back
    • ISO 22000
      • TEAM LEADER
      • INTRODUCTION
      • MASTERING
      • INTERNAL AUDITOR
      • TEMPLATES
      • Back
    • FDA COURSES
    • BETTER PROCESS CONTROL SCHOOL
      • ACIDIFIED
      • ASEPTIC
      • RETORT
      • ACIDIFIED + RETORT
      • Back
    • TRAIN PRODUCTION WORKERS
      • Employee Training Package
      • Back
    • INTERNAL AUDITS
      • SQF
      • FSSC 22000
      • BRCGS
      • ISO 22000
      • ISO 9001
      • Back
    • Back
  • COSMETICS
    • MoCRA
    • GMP (ISO 22716)
    • QUALITY TRAINING PACKAGES
    • ISO 9001 for COSMETICS
    • NON-CLINICAL GLP
    • PRESERVATIVE EFFICACY TESTING
    • Back
  • DRUGS
  • MEDICAL DEVICES
    • ISO 13485
      • INTRODUCTION
      • IMPLEMENTING
      • Back
    • EU MDR
    • Back
  • CONTACT