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HACCP Course Guide
HACCP Course Guide
Go GUIDE
On-the
TM
Contents
Getting Started . ........................................................................ 2 Step 7: Determine Critical Control Points (Principle 2)....95
7A | Preventing or Eliminating Food Safety Hazards..................... 96
HACCP Foundations................................................................. 3
7B | Using Decisions Trees FORM 8................................................. 101
A | Learning Objectives........................................................................ 8
7C | Form 8 Practical Examples Canned Mushrooms................... 105
B | Terminology....................................................................................... 9
7D | Unaddressed Hazards FORM 9................................................. 111
C | History................................................................................................ 14
7E | Revising Other Forms................................................................... 112
D | Benefits & Role of Management.................................................. 17
Takeaways............................................................................................... 116
E | Prerequisites..................................................................................... 20
F | Steps & Principles............................................................................ 23 Step 8: Establish Validated Critical Limits for Each CCP
G | Takeaways......................................................................................... 27 (Principle 3)................................................................................. 117
Step 1: Assemble a HACCP Team..........................................28 8A | Valid Critical Limits....................................................................... 118
1A | The Multidisciplinary Team......................................................... 29 8B | HACCP Plan FORM 10................................................................ 120
1B | Team Roles & Scope..................................................................... 30 Takeaways............................................................................................... 121
Takeaways............................................................................................... 31 Step 9: Establish a Monitoring System for Each CCP
Step 2: Describe the Product..................................................32 (Principle 4)................................................................................. 122
2A | Preparing the Product Description FORM 1.......................... 33 9A | Monitoring CCPs........................................................................... 123
2B | Key Questions to Ask................................................................... 37 9B | HACCP Plan FORM 10................................................................ 125
Takeaways............................................................................................... 38 Takeaways..................................................................................................... 126
Step 3: Identify Intended Use.................................................39 Step 10: Establish Corrective Action (Principle 5).............127
3A | How the Product Is Used FORM 1........................................... 40 10A | Actions to Take............................................................................ 128
3B | Product Ingredients & Incoming Materials FORM 2............. 43 10B | Corrective Action Records FORM 10.................................... 129
Takeaways............................................................................................... 45 Takeaways............................................................................................... 131
Step 4: Construct a Flow Diagram Describing the Process Step 11: Validate the HACCP Plan and Then Establish
.................................................................................................. 46 Verification Procedure (Principle 6)......................................132
4A | Flow Diagram................................................................................. 47 11A | Verification vs. Validation.......................................................... 133
4B | Plant Schematics........................................................................... 49 11B | The Validation Process.............................................................. 134
Takeaways............................................................................................... 51 11C | The Verification Process............................................................ 135
11D | Triggering a HACCP Plan Review ........................................... 136
Step 5: Onsite Confirmation of the Flow Diagram............52
11E | Documenting & File Management FORM 10...................... 137
5A | Conducting Inspections............................................................... 53
Takeaways............................................................................................... 139
5B | Quick Review Steps 1 - 5............................................................ 54
Takeaways............................................................................................... 59 Step 12: Establish Documentation & Recordkeeping
Step 6: Conduct Hazard Analysis and Define Control (Principle 7)................................................................................. 140
12A | Adequacy & Adherence............................................................. 141
Measures (Principle 1).............................................................. 50
12B | Making Note of Records FORM 10........................................ 143
6A | Types of Hazards........................................................................... 62
Takeaways............................................................................................... 144
6B | Identification of Hazards............................................................. 67
6C | Hazard Analysis Resources......................................................... 68 Answer Key ................................................................................ 145
6D | Risk Assessment............................................................................ 69
6E | Control Measures.......................................................................... 70
6F | FORM 5: Biological Hazards Identification............................. 72
6G | FORM 6: Chemical Hazards Identification............................. 79
6H | FORM 7: Physical Hazards Identification............................... 86
6I | Revising Other Forms.................................................................... 92
Takeaways............................................................................................... 94
We’ve designed this course with your convenience in mind, allowing you to move at your
own pace.
Typically, it takes approximately two to three hours to complete. Feel free to navigate
back and forth as needed through the various sections to ensure you are comfortable
with the course content.
And don’t worry we’ll test you too, with our HACCP Step and Principles Challenge Game.
Term 1
Control (noun)
To state wherein correct procedures are being followed and criteria are being met.
For example:
• During the health inspection, the inspector observed the food handlers wearing gloves, using
hairnets, and following proper hygiene practices.
• The food handlers followed the correct “control” meaning the right procedures and safety criteria
were met.
Term 2
Control Measure
Any action and activity that can be used to prevent or eliminate a food safety hazard or reduce it to an
acceptable level.
For example:
• In a production area, where cross-contamination is a concern, a control measure is to designate
separate cutting boards: red cutting board for meat and green one for vegetables.
•This action helps prevent the potential hazards of bacterial cross contamination.
Term 3
Corrective Action
Any action to be taken when the results of monitoring at the CCP indicate a loss of control or
deviation.
For example:
• At a critical control point where cooked chicken is supposed to reach a minimum of 75 degrees
Celsius, the temperature reading was found to be 69 which is below the required level (critical
limit).
• The corrective action taken was to keep cooking the chicken until the core temperature reaches
the proper temperature as set in the HACCP plan.
For example:
• In the corrective action example of the cooking chicken for 75 degrees Celsius to reduce the
number of harmful bacteria to a save level.
• Therefore, cooking is a Critical Control Point. Because it is the step that is essential to control the
biological hazard.
Term 5
Flow Diagram
A systematic representation of the sequence of steps or operations used in the
production or manufacture of a particular food item.
For example:
The steps for cooking chicken, starting from: receiving raw chicken, storing,
preparing, cooking, packing, and labelling.
Term 6
HACCP
A system which identifies, evaluates, and controls hazards which are significant for food safety.
Term 7
HACCP Plan
A document prepared in accordance with the principles of HACCP to ensure control of hazards which
are significant for food safety in the segment of the food chain under consideration.
For example:
A HACCP plan for a seafood industry will document the actions required for frequent temperature
checks, proper process steps, storage conditions, and cooking records to ensure food safety in the
seafood preparation process.
Term 9
Significant Hazard
A hazard within a food product or its environment that possesses a higher likelihood and severity of
causing adverse health effects, necessitating specific controls and preventive measures to mitigate its
impact on consumer safety.
Term 10
Hazard Analysis
The process of collecting and evaluating information on hazards and conditions leading to their
presence to decide which are significant for food safety and therefore should be addressed in the
HACCP plan.
For example:
Hazard Analysis for a Salad Production Process
In a salad production facility, a hazard analysis is conducted to identify potential risks to food safety.
One of the steps in the process is washing and chopping vegetables. During the hazard analysis, the
following hazards and conditions are evaluated.
Term 11
Microbiological Hazard
There is a risk of vegetables being contaminated with harmful bacteria, such as E. coli or Salmonella, if
they are not properly washed.
Term 12
Chemical Hazard
If employee didn’t follow the right procedure for the use of chemical sanitizer and its concentration to
wash the vegetable and rinse them properly.
Term 13
Physical Hazard
There’s a possibility of foreign objects like small stones or dirt being present in the vegetables if they
are not thoroughly inspected during washing.
Term 14
Validation
Obtaining evidence that the elements of the HACCP plan are effective. Validation is a one-
time process conducted to confirm the effectiveness of the chosen critical limit. In contrast, the
verification process occurs with each production cycle or batch, where the plant employees verify the
pasteurization temperature of 70 degrees is consistently met.
11 Introduction to HACCP Principles Building a Strong Foundation
Term 15
Verification
The application of methods, procedures, tests and other evaluations, in addition to monitoring to
determine compliance with the HACCP plan.
For example:
Consider a dairy processing plant that is introducing a new pasteurization process with a
pasteurization critical limit is 70 degrees Celsius. Validation involves conducting challenging tests to
ensure that 70 degrees Celsius is effective in reducing biological hazards to an acceptable level.
On the other hand, verification are all the methods and procedures that the plant must implement
to monitor the pasteurization process and ensure compliance with the critical limit established (70
degrees Celsius).
Matching 1
Can you match the term to its description?
HACCP
True or False
A risk assessment is any biological, chemical, or physical agent in food that can cause harm to
consumers?
TRUE FALSE
HACCP is globally recognized as a systematic and preventive approach that deals with
biological, chemical, and physical hazards by anticipating and preventing them, rather
than relying solely on end-product inspection and testing.
• In the 1950s, the first significant breakthrough in • The second breakthrough was the development of
quality management was linked to W.E. Deming, the HACCP concept itself.
renowned for his theories in this field.
• Created by the Pillsbury company in 1960, this
• His ideas greatly enhanced the quality of Japanese concept originated when NASA aimed for a “Zero
products. Defects” program to ensure the safety of astronaut
food in space.
• Dr. Deming and his contemporaries developed
total quality management (TQM) systems, which • Pillsbury adopted HACCP as a system that could
emphasized a comprehensive manufacturing offer maximal safety while diminishing reliance on
approach that improved quality and reduced costs end-testing and inspection.
simultaneously.
• Pillsbury publicly introduced the HACCP concept at
a 1971 food protection conference.
1993-1997
During the Codex Alimentarius
1950 1974 Commission held in Geneva, Switzer-
land, it was adopted. The commission
W.E. Deming and his The United States Food and Drug stated that the draft revision of General
colleagues develop Total Administration (FDA) incorporated HACCP Principles of Food Hygiene would
Quality Management (TQM) into regulations for Low-acid canned food. integrate HACCP principles. In 1997,
the General Principles of Food Hygiene
CAC/RCP 1 -1969, Rev (1997) was
established.
1960-1971 1985
The Pillsbury Company applies Numerous groups had
NASA ‘s zero defect approach embraced HACCP
and introduces the term to the
industry.
TRUE VS FALSE
A HACCP principles are internationally G HACCP is your shield against numerous food
recognized and can be applied globally. safety risks.
B HACCP promotes financial gain. H ‘Control measure’ was developed for use in the
C HACCP can improve the quality and food industry by NASA (1970s).
consistency of food products. I HACCP encourages a proactive approach to
D HACCP is only applicable to large food food safety issues.
manufacturing companies. J HACCP originated with W.E. Demining’s quality
E HACCP reduces the need for end-product management theories (1950s).
testing and inspection. K HACCP encourages a reaactive approach to
F Cross-contamination helps identify and prevent food safety issues.
potential hazards.
Open Doors to New Markets: Ensures Regulatory Compliance: Builds and Maintains Customer
Expand your horizons with Compliance with food safety Trust:
HACCP. It paves the way for regulations is non-negotiable. HACCP reinforces your
entering new markets, tapping HACCP is your compass, guiding dedication to delivering safe,
into fresh opportunities, and you to full compliance, protecting trustworthy food products. It’s a
diversifying your reach while your reputation, and ensuring promise that resonates with your
retaining existing customers. legal adherence. customers, fostering trust and
loyalty.
Key factors for success include management commitment and the allocation of necessary resources like
finances, time, and personnel. For instance, assembling the HACCP team with knowledgeable personnel from
various departments is crucial to expedite process.
In many cases, companies seek external technical support such as consultants, university professors or other
professional to assist in the development and implementation of their HACCP system.
TRUE VS FALSE
GMPs - GHPs
HACCP Good Manufacturing Practice Program (GMP)
is one of the prerequisite programs that are
commonly implemented in food facilities before
implementing and developing HACCP.
PREREQUISITE PROGRAM
(GMPS – GHPS) In this course, we will also refer to Good Hygiene
Practice (GHPs) which is a set of practices and
guidelines that are established to maintain a hy-
gienic and safe environment in food production,
handing and processing. GHP is an essential
component of food safety management and is
designed to prevent contamination, ensure the
quality of food products, and protect consumers
from potential health risks.
These examples represent just a subset of the various prerequisites programs that can be implemented to create a strong
foundation for a successful HACCP system. Each of these programs contributes to creating an environment that supports
the production of safe and high-quality food and present the base to build the HACCP system.
Good Manufacturing Practice Program (GMP) is a Good Hygiene Practices (GHPs) is a set of practices
set of guidelines, standards, and practices that are and guidelines that are established to maintain a
established to ensure the consistent and reliable hygienic and safe environment in food production,
production of safe, high-quality, and effective handling, and processing. GHP is an essential
products. component of food safety management and is
designed to prevent contamination, ensure the
quality of food products, and protect consumers from
potential health risks.
Sorting Activity
Can you distinguish good personal practice from bad personal practice?
1. Smoking in
designated area
A
Example of 2. Employee covering his
good personal beard with a beard net
practices
3. Uniform worn in
lunch room
B
Example of 5. Chewing gum at
bad personal work station
practices
6. Wearing jewelry
The 7 HACCP
Principles
Matching
Can you help Elena to match the HACCP principle
to the step?
Assemble a
HACCP Team
Learning
Objectives
By the end of Step 1:Assemble the HACCP Team you should be able to:
2
Describe the scope and responsibilities of the HACCP team.
To learn more about NOS for Food Safety and Quality Assurance Manager in the Food and Beverage
Manufacturing Industry visit the link : Skills Library
Multidisciplinary Management
is key Commitment
A multidisciplinary team is Management commitment will
essential when it comes to HACCP. make or break the success of
the implementation of a HACCP
program.
Describe the
Product
Learning
Objectives
By the end of Step 2: Describe the Product you should be able to:
3 Describe questions the HACCP team should ask before filling out HACCP Form 1: Product
Description Template.
u Composition u Labeling
u Physical/chemical Structure (including water u Shelf Life
activity, salt concentration, and pH). u Storage Conditions
u Packaging u Method of Distribution
IMPORTANT PRODUCT
CHARACTERISTICS OF (water activity, pH, etc.)
END PRODUCT
SPECIAL DISTRIBUTION
(shipping conditions)
CONTROL
Form Fields
Answer the questions below to ensure you are familiar with the specific fields in Form 1.
A. Product Name
B. Important Product
Characteristics of
the End Product
C. Shelf Life
C. Labelling
Instruction
Identify
Intended Use
Learning
Objectives
By the end of Step 3: Identify Intended Use you should be able to:
1 Describe the necessary fields on a completed HACCP Form 1: Product Description Template.
Describe the importance of filling out HACCP Form 1: Product Description Template to
2 prevent potential harm to consumers.
Describe the purpose of completing HACCP Form 2: Product Ingredients and Incoming
3
Materials Template.
IMPORTANT PRODUCT
CHARACTERISTICS OF (water activity, pH, etc.)
END PRODUCT
SPECIAL DISTRIBUTION
(shipping conditions)
CONTROL
The development of the HACCP plan must take in consideration if the product will be sold to elderly population,
such as in retirement homes or to immune compromised patients.
Matching Scenario. Imagine you and the HACCP team are preparing HACCP Form 1:
Product Description for your company’s canned mushrooms food processing line.
The multidisciplinary team has collected some critical information, evidence-based information
about your canned mushrooms. Where should the HACCP team place this information on
HACCP Form 1: Product Description?
HOW THE PRODUCT (i.e., ready to eat, further B. Water activity > 0.85 (high
IS TO BE USED processing required, heating, etc.)
moisture)
(packaging materials and
PACKAGING packaging conditions e.g.,
modified atmosphere)
C. Two years, at normal retail
(including storage temperature,
SHELF-LIFE
humidity if applicable) shelf temperatures
SPECIAL DISTRIBUTION
CONTROL
(shipping conditions) E. No physical damage, excess
humidity or temperature
DATE: APPROVED BY: extremes
FORM 2
PRODUCT INGREDIENTS AND INCOMING MATERIALS
PRODUCT NAME(S)
As a result, the HACCP team needs to sign off on all the forms
as part of the approval process. This ensures that everything is
in order before moving forward in the HACCP system.
Form Fields
Take some time to answer the questions below to practice filling out HACCP Form 2: Product
Ingredients & Incoming Materials Template.
The Scene. The HACCP team is now wanting to document the product ingredients and
incoming materials on HACCP Form 2: Product Ingredients & Incoming Materials Template. In
the case of your team’s canned mushroom product, you have four main product types you have
identified together:
Matching Question. Can you make an educated guess about the specifics of each of
your product categories and place them on the appropriate lines on HACCP Form 2: Product
Ingredients & Incoming Materials Template, based on the canned mushroom case study.
FORM 2
PRODUCT INGREDIENTS AND INCOMING MATERIALS
Construct a
Flow Diagram
Describing the
Process
Learning
Objectives
By the end of Step 4: Construct a Flow Diagram Describing the Process you should be able to:
1 Describe the process of constructing a flow diagram describing the process on HACCP Form
3: Flow Diagram Template.
Describe the process of constructing a plant schematic during HACCP Step 4: Construct a
2
Flow Diagram Describing the Process.
MUSHROOM WATER
EMPTY CANS DRY INGREDIENTS
(RAW) (MUNICIPAL)
20. Weighing
22. Head-Spacing
26. Cooling
27. Conveying/Drying
28. Labelling/Storing
29. Shipping
For Example
To mark the end of HACCP Step 4: Construct a Flow Diagram Describing the Process, the HACCP Team must
complete HACCP Form 4: Plant Schematic or Floor Plan.
Reference Preventive Control Plan Templates for Domestic Food Businesses - Canadian Food Inspection Agency
Onsite
Confirmation
of the Flow
Diagram
Learning
Objectives
By the end of Step 5: Onsite Confirmation of Flow Diagram you should be able to:
Describe the inspection process during HACCP Step 5: Onsite Confirmation of Flow
1
Diagram.
Forms 1-4
Finally, we completed the forms 1, 2, 3 and 4 required for the first 5 steps. And we used Canned
mushroom as a practical example.
u HACCP Form 1: Product Description u HACCP Form 3: Flow Diagram
u HACCP Form 2: Product Ingredients & u HACCP Form 4: Plant Schematic or Floor Plan
Incoming Materials
MUSHROOM WATER
EMPTY CANS DRY INGREDIENTS
(RAW) (MUNICIPAL)
1. Receiving 1. Receiving 3. Receiving 4. Intaking DATE: Aug 17, 2023 APPROVED BY: HACCP team
5. Storing 6. Storing 7. Storing
20. Weighing
22. Head-Spacing
26. Cooling
27. Conveying/Drying
28. Labelling/Storing
29. Shipping
1. Design marketing
campaigns
1. The packaging
materials used and the
product shelf life
2. The various
HACCP Step 2 characteristics of each
What is included in the ingredient used
HACCP product description?
3. The packaging
materials and the
product shelf-life
4. The product’s
marketing and sales
strategy
2. A rough estimation of
HACCP Step 3 the composition of the
What should the ‘intended product
use of a product’ be based
on?
3. The known uses by the
end user or consumer
1. The facility’s
water intake.
HACCP Step 4
2. Flow of ingredients and
packaging materials
When preparing a plant
schematic, what crucial
aspects does it help
identify and manage within
3. The preferred color
scheme for the facility a food facility?
1. To design marketing
materials for the
product
4. To establish the
product’s price point
Conduct
Hazard Analysis
and Define Control
Measures
Learning
Objectives
By the end of Step 6: Conduct Hazard Analysis and Define Control Measures you should be able to:
Navigate CFIA’s Reference Database for Hazard Identification (RDHI) to perform a hazard
3
analysis.
6 Identify the fields and processes the HACCP team needs to adequately fill out on HACCP
Forms 5-7.
Describe the process of updating HACCP Form 2: Product Ingredients and Incoming
7
Materials, and HACCP Form 3: Flow Diagram, following the completion of HACCP Forms
5-7.
Biological Hazards
Biological hazards are those living organisms that may
cause illness if they or their products (e.g. toxins) are
ingested.
• Incoming ingredients, including raw materials such as raw poultry and raw meat
• Cross-contamination in the processing or storage environment. For example, if the same cutting board and knife are used to chop
raw chicken and to cut the vegetables without proper cleaning and sanitization in between, cross-contamination can occur. Because
harmful bacteria such as Salmonella or Campylobacter, who are present on the raw chicken, could be transferred to the vegetables
though the cutting board and knife.
• mployees who are not following proper hygiene practices or are themselves carrying infectious agents can contaminate the food
E
with biological hazards.
• ood contact surfaces, such as cutting boards, utensils, and equipment, can harbor harmful microorganisms if not properly cleaned
F
and sanitized, leading to contamination of the food.
• ests, such as insects and rodents, can carry and spread disease-causing microorganisms. If pests have access to food storage or
P
preparation areas, they can contaminate the food with biological hazards.
Overall, these examples highlight the diverse ways in which biological hazards can enter the food production process and contaminate
the food. Preventing and managing these hazards through the control measures in the GMPs and GHPs is crucial to ensuring food safety.
Chemical Hazards
Sanitation chemicals (cleaners, sanitizers) and equipment
maintenance chemicals (lubricants, machine oils) are
common sources of chemical hazards if not controlled well.
Physical Hazards
Physical hazards are objects found in food that can cause
injury to the consumer. Physical hazards can be from the
environment or could be part of the food itself.
Dirty vehicles, cross contamination Poor sanitation practices will Outdoor pollution, design and/or
with maintenance chemicals, not only cause introduction construction of a building, type
foreign material or allergens can of biological but also chemical of material used, condition of the
also cause product contamination. hazards if not controlled. Not building can also contaminate the
rinsing the equipment properly product. The hazard associated
after sanitation chemical with those resources is not the
application will definitely lead to same if the production room
introduction of chemical hazard. walls are made of wood or plastic
panels. You can guess that it is
much easier to clean, sanitize
and maintain plastic rather then
wood.
u C ould these materials harbor harmful u C ould using certain ingredients in amounts
microorganisms, toxins, chemicals, or foreign lower than recommended, or omitting them
objects? Are preservatives or additives used to entirely, lead to hazards due to microbial
eliminate microorganisms, hinder their growth, growth (e.g., nitrite levels in bacon)?
or extend shelf life? u Do the final product’s moisture content and
u Could any ingredients become hazardous if water activity influence microbial growth or
excessively used? (For instance, excessive the survival of pathogens?
nitrites in bacon could pose a chemical risk.) u Does the ingredient list include allergens?
#2 Processing
A similar approach goes to identify hazards in processing steps.
For further guidance, check out the CFIA’s resource on Conducting a Hazard Analysis. CFIA (2019)
Put simply, the concept of risk assessment answers the fundamental questions:
Control measures need to be validated, which is obtaining Control measures are defined as any
evidence that a control measure of combination of control, if actions or activities that can be used to
properly implemented, is capable of controlling the hazard to prevent or eliminate a food safety hazard
a specific outcome. or to reduce it to an acceptable level.
CONTROLLING BIOLOGICAL
HAZARDS
CONTROLLING PHYSICAL
HAZARDS
FORM 5 HAZARD ID
CONTROLLED AT
IDENTIFIED BIOLOGICAL HAZARDS
(control measures)
1 MUSHROOM
(RAW)
EMPTY CANS 2 DRY INGREDIENTS 3 WATER
(MUNICIPAL) 4
1. Receiving 1. Receiving 3. Receiving 4. Intaking
20. Weighing
22. Head-Spacing
26. Cooling
27. Conveying/Drying
28. Labelling/Storing
29. Shipping
Let’s Practice
Let’s practice putting the information on HACCP Form 5: Biological Hazard Identification.
PROCESS STEPS
A. P
resence of Clostridium botulinum, yeast or B. G
rowth of thermophilic bacteria due to
molds. improper cleaning of the blancher.
PROCESS STEPS
A. C
ontamination by rodent excrement. B. S
urvival of pathogenic bacteria due to non-
validated process.
MUSHROOM WATER
EMPTY CANS DRY INGREDIENTS
(RAW) (MUNICIPAL)
20. Weighing
22. Head-Spacing
26. Cooling
27. Conveying/Drying
28. Labelling/Storing
29. Shipping
A. P
ost-process B. S
urvival of pathogenic due C. Post-process
contamination with to improper flow patterns contamination due to
pathogenic bacteria due to allowing bypass of thermal insufficient or excessive
inadequate blanching. process. cooling causing can
leakage.
Controlled at CCP5B
Presence of spores
(25.thermal processing)
Dry ingredients
GMPs Pest control
Contamination by rodent excrement
program
Water Presence of microorganisms such as coliform, spore forming bacteria, viruses, parasites GMPs Premises
Controlled at CCP4B
Could arrive with serious internal double seam or body plate defects , leading to leakage
(23.End feeding/
and post process contamination
closing/inspection)
Empty cans and ends
Controlled at CCP1BP
Could arrive with serious external double seam, Body plate lacquer coating defects, or
(9. can inspecting/
damage, resulting in leakage and post process contamination
depalletizing)
PROCESS STEPS
Refrigerated
Multiplication of bacterial load due to improper storage temperature & humidity GMPs Equipment
mushroom storing
Growth of thermophilic bacteria due to improper cleaning of the blancher
GMPs Sanitation &
Mushroom blanching Post process contamination with pathogenic bacteria due to inadequate blanching
Equipment
Inadequate thermal processing due to textural changes from excessive blanching
Contamination from improper flow patterns in processing area, allowing heat processed
cans being contaminated with unclean water from unprocessed baskets of cans
Survival of pathogenic due to improper flow patterns allowing bypass of thermal process GMPs process control
Thermal processing CCP5B
Survival of pathogenic bacteria after thermal processing due to excessive time lapse
between closing and retorting
Survival of pathogenic bacteria caused by inadequate heat treatment from not following
time, temperature, and other critical factors of the scheduled process
1 MUSHROOM
(RAW)
EMPTY CANS 2 DRY INGREDIENTS 3 WATER
(MUNICIPAL) 4
1. Receiving 1. Receiving 3. Receiving 4. Intaking
20. Weighing
22. Head-Spacing
26. Cooling
27. Conveying/Drying
28. Labelling/Storing
29. Shipping
Let’s Practice
Let’s practice putting the information on HACCP Form 6: Chemical Hazards Identification.
PROCESS STEPS
A. C
ould be contaminated with grease or oils B. C
ontamination of mushrooms from cleaning
or cleaning chemicals. chemical residues.
PROCESS STEPS
A. C
ontamination from chemical cleaning B. C
ontamination by pesticide residues.
during cleaning and sanitation procedures.
MUSHROOM WATER
EMPTY CANS DRY INGREDIENTS
(RAW) (MUNICIPAL)
20. Weighing
22. Head-Spacing
26. Cooling
27. Conveying/Drying
28. Labelling/Storing
29. Shipping
A. C
ontamination from chemical cleaning B. C
ontamination of mushrooms from cleaning
during cleaning and sanitation procedures. chemical residues.
Water Presence of environmental contaminants (e.g., heavy metals or toxic substances) GMPs Premises
GMPs Receiving,
Empty cans and ends Could be contaminated with grease or oils or cleaning chemicals storage and
transport
PROCESS STEPS
Refrigerated
Contamination from chemical cleaning during cleaning and sanitation procedures GMPs Sanitation
mushroom storing
Mushroom blanching Contamination of mushrooms from cleaning chemical residues GMPs Sanitation
1 MUSHROOM
(RAW)
EMPTY CANS 2 DRY INGREDIENTS 3 WATER
(MUNICIPAL) 4
1. Receiving 1. Receiving 3. Receiving 4. Intaking
20. Weighing
22. Head-Spacing
26. Cooling
27. Conveying/Drying
28. Labelling/Storing
29. Shipping
Let’s Practice
Let’s practice putting the information on HACCP Form 7: Physical Hazards Identification.
PROCESS STEPS
MUSHROOM WATER
EMPTY CANS DRY INGREDIENTS
(RAW) (MUNICIPAL)
20. Weighing
22. Head-Spacing
26. Cooling
27. Conveying/Drying
28. Labelling/Storing
29. Shipping
A. C
ontamination by harmful extraneous B. C
ontamination by metal fragments from
materials. plant machinery.
GMPs Receiving,
Dry ingredients Presence of harmful extraneous materials, such as glass, metal, plastic, or wood
Storing and Transport
GMPs Receiving,
Empty cans and ends Contaminated by metal fragments
Storing and Transport
PROCESS STEPS
1 MUSHROOM 2 3 WATER 4
EMPTY CANS DRY INGREDIENTS
(RAW) (MUNICIPAL)
20. Weighing
22. Head-Spacing
26. Cooling
27. Conveying/Drying
28. Labelling/Storing
29. Shipping
ASCORBIC ACID
B Biological Hazard
C Chemical Hazard
CITRIC ACID
B Biological Hazard
C Chemical Hazard
MUSHROOM WATER
EMPTY CANS DRY INGREDIENTS
(RAW) (MUNICIPAL)
P 1. Receiving 1. Receiving P 3. Receiving P 4. Intaking
B - BIOLOGICAL HAZARD
C - CHEMICAL HAZARD
P - PHYSICAL HAZARD
Takeaways A Critical
C
B P B P B P
C C C
P B P
C
Determine
Critical Control
Points
Learning
Objectives
By the end of Step 7: Determine Critical Control Points you should be able to:
Describe the high level processes the HACCP team follows during HACCP Step 7: Critical
1 Control Points.
2 Describe the process of using decision trees during the HACCP process.
Describe the process required to fill out HACCP Form 8: CCP Determination and HACCP
3 Form 9: Unaddressed Hazards.
4 Describe the process of revising HACCP Forms 5-7 in light of the findings on HACCP Form 8
& 9.
95 Introduction to HACCP Principles Building a Strong Foundation
Preventing or
7A
Eliminating Food Safety Hazards
Let’s look at the importance of hazard prevention and
elimination
Controlling Hazards
Controlling hazards can be achieved
through two approaches:
By using a decision
By implementing a tree to determine
GMP program. if a step qualifies
as a CCP.
2 Completing HACCP Form 8: CCP Determination and HACCP Form 9: Unaddressed Hazards.
Updating and reviewing HACCP Form 5: Biological Hazard Identification, HACCP Form
3 6: Chemical Hazard Identification, and HACCP Form 7: Physical Hazard Identification to
confirm whether the hazards identified can be effectively controlled by existing GMPs or if
more specific control and monitoring are required.
Controlled at CCP5B
Presence of spores
(25.thermal processing)
Dry ingredients
GMPs Pest control
Contamination by rodent excrement
program
Water Presence of microorganisms such as coliform, spore forming bacteria, viruses, parasites GMPs Premises
Controlled at CCP4B
Could arrive with serious internal double seam or body plate defects , leading to leakage
(23.End feeding/
and post process contamination
closing/inspection)
Empty cans and ends
Controlled at CCP1BP
Could arrive with serious external double seam, Body plate lacquer coating defects, or
(9. can inspecting/
damage, resulting in leakage and post process contamination
depalletizing)
PROCESS STEPS
Refrigerated
Multiplication of bacterial load due to improper storage temperature & humidity GMPs Equipment
mushroom storing
Growth of thermophilic bacteria due to improper cleaning of the blancher
GMPs Sanitation &
Mushroom blanching Post process contamination with pathogenic bacteria due to inadequate blanching
Equipment
Inadequate thermal processing due to textural changes from excessive blanching
Contamination from improper flow patterns in processing area, allowing heat processed
cans being contaminated with unclean water from unprocessed baskets of cans
Survival of pathogenic due to improper flow patterns allowing bypass of thermal process GMPs process control
Thermal processing CCP5B
Survival of pathogenic bacteria after thermal processing due to excessive time lapse
between closing and retorting
Survival of pathogenic bacteria caused by inadequate heat treatment from not following
time, temperature, and other critical factors of the scheduled process
Water Presence of environmental contaminants (e.g., heavy metals or toxic substances) GMPs Premises
GMPs Receiving,
Empty cans and ends Could be contaminated with grease or oils or cleaning chemicals storage and
transport
PROCESS STEPS
Refrigerated
Contamination from chemical cleaning during cleaning and sanitation procedures GMPs Sanitation
mushroom storing
Mushroom blanching Contamination of mushrooms from cleaning chemical residues GMPs Sanitation
GMPs Receiving,
Dry ingredients Presence of harmful extraneous materials, such as glass, metal, plastic, or wood
Storing and Transport
GMPs Receiving,
Empty cans and ends Contaminated by metal fragments
Storing and Transport
PROCESS STEPS
CANNED MUSHROOMS
INCOMING
Mushrooms
INGREDIENTS
Q1 Do control preventive
measure(s) exist?
Modify step,
No process or
Yes product
Q2
Is the step specifically designed to
eliminate or reduce likely or occurrence Yes
of a hazard to an acceptable level?
No
Q3
Could contamination with identified hazard(s) occur
in excess or acceptable level(s) or could these
increase to unacceptable levels?
Q4
Will a subsequent step eliminate
identified hazard(s) or reduce likely
occurrence to an acceptable level?
Question 1
Do control preventive measure(s) exist?
Q1 Do control preventive
measure(s) exist?
Modify step,
2 No process or
1 Yes product
1. YES 2. NO 3. NO 4. YES
If the HACCP team’s answer If the HACCP team’s answer to Note that if the control isn’t If the answer to “Is the control
to Q1 is yes, then they can go Q1 is no, then they must ask necessary for safety than it is at this step necessary for
directly to question 2 on the several questions in succession not a CPP. safety?” is yes, the HACCP
tree diagram. the first being: “Is the control at team must modify the step,
this step necessary for safety?” process, or product.
Basically within the context of all HACCP plans, the answer to question 1 is almost universally, “YES”. This is due
to the inherent presence of control measures establish with the GMPs, which actively protect and prevent the
food from hazards.
Question 2
Is the step specifically designed to eliminate or reduce the likely occurrence of a hazard to an acceptable level?
Q2
Is the step specifically designed to
eliminate or reduce likely or occurrence Yes 2
of a hazard to an acceptable level?
1 No
Q3
Could contamination with identified hazard(s) occur
in excess or acceptable level(s) or could these
increase to unacceptable levels?
Additional examples include the chlorination of cooling water, which serves to control both biological and
chemical hazards. Another instance is to use metal detector to eliminate physical hazard/metals fragment.
Question 3
Could contamination with identified hazards occur in excess of acceptable level(s) or could these increase to
unacceptable levels?
Q3
Could contamination with identified hazard(s) occur
in excess or acceptable level(s) or could these
increase to unacceptable levels?
Q4
Will a subsequent step eliminate
identified hazard(s) or reduce likely
occurrence to an acceptable level?
1. YES 2. NO
If the HACCP team’s answer to If the HACCP team’s answer
Q3 is yes, then they must go to to Q3 is no, then this is a not a
question 4 on the tree diagram. CCP and stop.
For example, cooling water chlorination. Could contamination with identified hazard(s) occur in excess of
acceptable level(s) or could these increase to unacceptable levels?
The answer is YES! If the cooling water chlorination is not properly maintained, there is a risk of excessive
bacterial growth. Go to question 4 for further assessment.
Question 4
Will a subsequent step eliminate identified hazard(s) or reduce likely occurrence to an acceptable level?
Q4
Will a subsequent step eliminate
identified hazard(s) or reduce likely
occurrence to an acceptable level?
The answer for Q3 is yes. Will a subsequent step eliminate the hazard or reduce likely occurrence to an
acceptable level? The answer is no and therefore, the pasteurization of milk is CCP.
Q1 Q3
Do control preventive Could contamination with identified hazard(s)
measure(s) exist? occur in excess or acceptable level(s) or
could these increase to unacceptable levels?
Q2 Q4
Is the step specifically designed to Will a subsequent step eliminate
eliminate or reduce likely or occurrence identified hazard(s) or reduce likely
of a hazard to an acceptable level? occurrence to an acceptable level?
Let’s Practice
Let’s practice using the decision tree questions on HACCP Form 8: CCP Determination.
Q1 Q3
Do control preventive Could contamination with identified hazard(s)
measure(s) exist? occur in excess or acceptable level(s) or
could these increase to unacceptable levels?
Q2 Q4
Is the step specifically designed to Will a subsequent step eliminate
eliminate or reduce likely or occurrence identified hazard(s) or reduce likely
of a hazard to an acceptable level? occurrence to an acceptable level?
1. Based on Form 8, what answers were provided by the HACCP team on decision tree
questions 1 - 4 for the biological hazard on dry ingredients?
3. Based on Form 8, what answers were provided by the HACCP team on decision tree
questions 1 - 4 for the biological hazard: post process contamination from serious external
defects.
1. N/A
2. N/A
3. N/A
4. Fully controlled by GMPs through Sanitation Program.
For the final physical hazards: harmful extraneous materials, GMPs alone are not sufficient.
There is a specific step, Step 9 (inspecting and depalletizing), designed to help eliminate this risk by identifying
and removing harmful extraneous materials from the process.
DRY
DRY
INGREDIENTS.
INGREDIENTS.
PHYSICAL: WATER.
BIOLOGICAL:
PRESENCE OF BIOLOGICAL &
CONTAMINATION
HARMFUL CHEMICAL
BY RODENT
EXTRANEOUS HAZARDS.
EXCREMENT.
MATERIALS.
This hazard is fully controlled This hazard is fully controlled These are fully controlled by
by GMPs through the pest by the GMPs through GMPs through facility and
control program. purchasing and delivering water supply requirements.
programs which include
supplier verification programs.
CANNED MUSHROOMS
INCOMING
Mushrooms
INGREDIENTS
Controlled at CCP5B
Presence of spores
(25.thermal processing)
Dry ingredients
GMPs Pest control
Contamination by rodent excrement
program
Water Presence of microorganisms such as coliform, spore forming bacteria, viruses, parasites GMPs Premises
Controlled at CCP4B
Could arrive with serious internal double seam or body plate defects , leading to leakage
(23.End feeding/
and post process contamination
closing/inspection)
Empty cans and ends
Controlled at CCP1BP
Could arrive with serious external double seam, Body plate lacquer coating defects, or
(9. can inspecting/
damage, resulting in leakage and post process contamination
depalletizing)
PROCESS STEPS
Refrigerated
Multiplication of bacterial load due to improper storage temperature & humidity GMPs Equipment
mushroom storing
Growth of thermophilic bacteria due to improper cleaning of the blancher
GMPs Sanitation &
Mushroom blanching Post process contamination with pathogenic bacteria due to inadequate blanching
Equipment
Inadequate thermal processing due to textural changes from excessive blanching
Contamination from improper flow patterns in processing area, allowing heat processed
cans being contaminated with unclean water from unprocessed baskets of cans
Survival of pathogenic due to improper flow patterns allowing bypass of thermal process GMPs process control
Thermal processing CCP5B
Survival of pathogenic bacteria after thermal processing due to excessive time lapse
between closing and retorting
Survival of pathogenic bacteria caused by inadequate heat treatment from not following
time, temperature, and other critical factors of the scheduled process
Water Presence of environmental contaminants (e.g., heavy metals or toxic substances) GMPs Premises
GMPs Receiving,
Empty cans and ends Could be contaminated with grease or oils or cleaning chemicals storage and
transport
PROCESS STEPS
Refrigerated
Contamination from chemical cleaning during cleaning and sanitation procedures GMPs Sanitation
mushroom storing
Mushroom blanching Contamination of mushrooms from cleaning chemical residues GMPs Sanitation
GMPs Receiving,
Dry ingredients Presence of harmful extraneous materials, such as glass, metal, plastic, or wood
Storing and Transport
GMPs Receiving,
Empty cans and ends Contaminated by metal fragments
Storing and Transport
PROCESS STEPS
Hazard Decision
Control Trees
Controlling hazards can be Decision trees have 4 important
achieved through 2 approaches: questions the team works to
implementing a GMP program and answer. Each question leads the
using a decision tree to determine team to a different intervention
if a step qualifies as a CCP based on if the answer is yes or no
to the questions.
Establish Validated
Critical Limits for
Each CCP
Learning
Objectives
By the end of Step 8: Establish Validated Critical Limits for Each CCP you should be able to:
Describe what makes a critical limit valid and credible resources for establishing critical limits
1 for each CCP.
2 Describe the process of filling out HACCP Form 10: HACCP Plan.
For Example;
Temperature, time, Pasteurization’s temperature and
Moisture level minimum exposure time is 75degree Celsius for at
duration least 15 seconds
Physical product
Available chlorine
dimensions
For Example;
Metal fragments larger than
0.5 mm
Conveyor belt speed Water activity
Maintaining these parameters
within specified boundaries is
Viscosity crucial, as it ensures the safety
conductance, flow of the product.
rate etc.
Examples
In the process of establishing critical limits, information from various sources can be gathered. Examples
including but not limited to the following:
If there is no existing published evidence to support that the proposed critical limits are effective in controlling
hazards at a CCP, it becomes necessary to conduct validation exercises. These may include mathematical and/or
microbiological modeling, supported by challenge testing or other relevant studies. The goal is to ensure that the
chosen critical limits are valid and effective in maintaining control over the hazard.
For further information, consult more advanced HACCP courses, where discuss further these details.
HAZARD
MONITORING PROCEDURES CORRECTIVE
PROCESS DESCRIPTION CRITICAL VERIFICATION
CCP # ACTIONS RECORDS
STEP / SIGNIFICANT LIMITS WHEN ACTIVITIES
WHAT HOW WHO PROCEDURES
HAZARD(S) (FREQUENCY)
The HACCP team have The biological hazards limit of 30 seconds between All these critical limits are
previously identified that can previously identified in the sealing and the retorting measurable and objective, as
inspecting/depalletizing step is other forms are survival of process to ensure safety. required by the definition of the
the first CCP for both biological pathogenic bacteria due to Please note that I used this critical limit.
and physical hazard, and we’ve bypass of thermal process, critical limit just as an example;
described these hazards in the excessive time laps between this type of critical limit may
previous forms. closing and retorting or vary for each production line
inadequate implementation of step.
The Critical limits for this heat treatment factors.
CCP is ensuring there are no 3. Time and temperature of
incorrect, damaged or defective The critical limits of these heat treatment: Once again
cans. This applies to both hazards are: fort the sake of this example,
biological as well as the physical we’ll set the critical limit at 110
hazards. 1. For bypass of thermal degrees celsisus for 5 minutes.
process: to confirm that the Again, this critical limit is very
The HACCP team has thermal process has taken unique and specific to each
established a “Zero Tolerance” place, we use a heat-sensitive process setup, can size and
policy, meaning there’s no room indicator that changes color. other variables.
for any damaged cans on the In this example, we’ll use a
production line. transparent indicator that turns Now, you have learned about
Establish a
Monitoring System
for Each CCP
Learning
Objectives
By the end of Step 9: Establish a Monitoring System for Each CCP you should be able to:
The monitoring procedure/method and frequency should be capable of timely detection of any deviation or
failure to remain whin critical limits, to allow timely isolation and evaluation of the product and avoid product
waste.
HAZARD
MONITORING PROCEDURES CORRECTIVE
PROCESS DESCRIPTION CRITICAL VERIFICATION
CCP # ACTIONS RECORDS
STEP / SIGNIFICANT LIMITS WHEN ACTIVITIES
WHAT HOW WHO PROCEDURES
HAZARD(S) (FREQUENCY)
Establish
Corrective Action
Learning
Objectives
By the end of Step 10: Establish Corrective Action you should be able to:
Describe the need for specific written corrective actions developed for CCP in the HACCP
1 plan, to effectively respond to deviations when they occur.
Recognize the importance of using corrective actions to bring CCPs under control and to
3
prevent unsafe food from reaching consumers.
Therefore, Corrective actions should be developed for each CCP in the HACCP plan in order to respond to
deviations from the Critical Limit when they occur.
CORRECTIVE ACTIONS
Corrective Actions for a critical limit deviation
can be categorized into two types.
1 2
CAUSE SPECIFIC
Target the root cause CORRECTIVE ACTIONS
of the problem which Corrective actions for a
minimizes the potential for critical limit deviation can
the deviation to reoccur. be categorized into two
For example, repairing types.
malfunctioning equipment.
Corrective Actions
Details of the corrective actions 2 The Product Disposition
3
should be documented in the
HACCP records, including: Reproducing Procedures
HAZARD
MONITORING PROCEDURES CORRECTIVE
PROCESS DESCRIPTION CRITICAL VERIFICATION
CCP # ACTIONS RECORDS
STEP / SIGNIFICANT LIMITS WHEN ACTIVITIES
WHAT HOW WHO PROCEDURES
HAZARD(S) (FREQUENCY)
Step 9: 1. Must remove any incorrect Step 25: The Retort Operator must
Inspecting/ cans, cans with serious defects Thermal adjust time/temperature
Depalletizing and damaged cans.
Processing of cook as per authorized
contingency Correction Action
The HACCP team now 2. Must inform QC The HACCP for CCP#5B Plan.
completes the correction action “thermal processing”, also
column on HACCP Form 10: 3. Must hold remainder of fills in the corrective action
HACCP Plan. pallets. procedures.
Verification Validation
Using
Review of Using Conducting guidance
scientific mathematical challenging developed by
literature models studies authoritative
sources
Testing
Plan Monitoring System
Plan Review
Establish sampling and testing
plan for microorganisms Establish facility environment Review the HACCP system,
(pathogens or their indicators), and monitoring plan for microbial including the hazard analysis and
chemical hazards such as contaminants such as Listeria. the HACCP plan, either through
mycotoxins or physical hazards internal audit or third-party
such as metal fragments, to verify audits.
product safety.
HACCP Triggers
Let’s look at some specific examples of what might trigger a HACCP review.
Trigger 1
New Product Line
Introducing a new product line, which demands either a new product-specific HACCP plan or modifications to
incorporate variations.
For instance, if you had a HACCP plan for chocolate bars and are now adding a new product line for pistachio
chocolate bars with different hazards, a review and a validation of the new plan is now required.
Trigger 2
Process Amendment
If a process changes, the HACCP plan no longer aligns with the production method, including altered flow
diagrams. This impacts the hazard analysis, necessitating a review and revalidation of the HACCP plan.
Trigger 3
Product Amendment
Product amendments, such as changes in intended use or usage instructions in Forms 1 and 2, also trigger a
comprehensive HACCP plan review and potential revalidation.
Trigger 4
Change in scientific knowledge of hazards
Changes in scientific knowledge regarding hazards, like the emergence of new pathogens impacting product
safety.
Trigger 5
Change in regulations
Changes in regulations, such as new legal limits for toxins (e.g., mycotoxins) or allergens (e.g., sulphites).
Trigger 6
Data analysis from trend or customer complaints
Data from trend analysis and customer complaints revealing system failures, indicating the need for a HACCP
plan review.
Recording
1 Verification Methods
Verification 2 Date
Activities
Verification activities must be 3 Individual Responsible
for Verification
recorded within the HACCP plan.
This should include the following
items: verification methods, 4 Responsible Individual/
Organization for Laboratory Results
5
date, individuals responsible for
verification, or the responsible Results or Findings
organization for laboratory results,
results or findings, and actions taken.
6 Actions taken
File Management
A verification procedure for the overall HACCP plan should be documented in a designated file. Any reviews or
revalidations of the HACCP plan must also be included in this file.
As mentioned earlier, a document control procedure should manage outdated HACCP documents. A similar
procedure should be developed for record management, referred to as the record control procedure. The final
HACCP principle will provide more detailed information on record control requirements.
HAZARD
MONITORING PROCEDURES CORRECTIVE
PROCESS DESCRIPTION CRITICAL VERIFICATION
CCP # ACTIONS RECORDS
STEP / SIGNIFICANT LIMITS WHEN ACTIVITIES
WHAT HOW WHO PROCEDURES
HAZARD(S) (FREQUENCY)
Learning
Objectives
By the end of Step 12: Establish Documentation & Recordkeeping you should be able to:
1 Describe key documents and records that must be kept as part of the HACCP program.
2 Identify the field where documents are recorded on HACCP Form 10: HACCP Plan.
Other support
documentation for
developing the HACCP
plan - guide
HAZARD
MONITORING PROCEDURES CORRECTIVE
PROCESS DESCRIPTION CRITICAL VERIFICATION
CCP # ACTIONS RECORDS
STEP / SIGNIFICANT LIMITS WHEN ACTIVITIES
WHAT HOW WHO PROCEDURES
HAZARD(S) (FREQUENCY)