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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

Before the Audit

Before the Registration / Certification Audit

Use and Improve your FSSC 22000 or SQF System.

Once you complete the design and implementation of the FSSC 22000 or SQF System, the next step in your project is to use and improve the system.

  1. Follow documented procedures and work instructions

    Everyone in your organization should be performing processes following your documented procedures and work instructions, complying with the documented requirements.

  2. Make improvements to the processes

    Many of these procedures may be new to your organization, or have changed significantly during your project. Now that they are actually in use, you will most likely find areas that can be improved. Make improvements using the Corrective Action process and the document revision process.

  3. Conduct Internal Audits

    Schedule internal audits to cover all areas of the organization before your Registration Audit. Train your Internal Auditors. Make sure you schedule at least one internal audit before your registration audit (we recommend 2 or more). Allow time to take corrective action on any findings. A robust and effective internal audit program is one of the best tools to finding and correcting shortcomings in the System before your Certification Audit.

  4. Hold frequent Management Review meetings

    Management Review is another key factor in getting the new FSMS ready for a Certification Audit. Review information from Internal Audits, Corrective Action and results of verification activities. Initiate corrective actions to fix problems and make improvements to the FSSC System.

  5. Keep records

    During the Certification Audit, the auditor will be looking for evidence that you are complying with the requirements of FSSC Standard or SQF Code and of your own procedures and work instructions. This evidence is in the form of records that you generate as you run your system. Be sure that you are following all of the records requirements that you set up in the system. Run your system for several months before your Certification Audit so there are sufficient records for the auditor to evaluate.

Featured Training

Complete Training Package

Food Safety

Complete Training Package

Food Safety

Implementing

FSSC 22000

Mastering

SQF

Understanding

FSSC 22000

Internal Auditor

Food Safety

Internal Auditor

Food Safety

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FSSC 22000 Quickstart Guide

FREE FSSC 22000 Quick Start Guide

Learn about FSSC 22000 and what you need to do to prepare your company for FSSC 22000 certification!
  • What is FSSC 22000?
  • Benefits of FSSC 22000 Implementation
  • Step-by-Step Explanations
  • Sample Implementation Timeline, Project Plan, Team Meeting Agendas
  • BONUS: Receive a series of FSSC 22000 how-to informational emails and more free FSSC 22000 downloads
GFSI PPT

What is GFSI & How to Get Certified

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Get a Limited Time Demo of RegiLearn

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Would you like to try out the training? We are so confident in our training that we'd like to let you try a chapter for free. Fill out this form and we will set up a test account for you.

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SQF Edition 9 Quickstart Guide

What is SQF & How to Get Certified

  • SQF Explained
  • Benefits of SQF
  • Step-by-Step Overview
  • Sample Timeline, Project Plan, Team Meeting Agendas
  • Informational emails about SQF implementation, with links to free downloads and online tools
  • 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