Food Safety Management system details and all the 7 priciples are disscussed in this power point slide show. you can learn a lot of content from this slide. here are the 7 basic principles of HACCAP. You can also learn about FSMS.
Food Safety Management system details and all the 7 priciples are disscussed in this power point slide show. you can learn a lot of content from this slide. here are the 7 basic principles of HACCAP. You can also learn about FSMS.
In an era where food safety is of paramount importance, HACCP has emerged as a systematic and preventive approach to identifying and managing potential hazards in food production processes. This presentation aims to shed light on the fundamental principles of HACCP, its benefits, and its significance in ensuring the safety of our food supply.
Definition and Background:
We begin by defining HACCP as an internationally recognized food safety management system designed to identify, evaluate, and control hazards that may pose risks to the safety of food products. It originated in the 1960s, developed by the Pillsbury Company in collaboration with NASA, with the primary objective of ensuring safe food for astronauts. Since then, HACCP has been widely adopted and applied across various sectors of the food industry.
Principles of HACCP:
Next, we delve into the seven core principles of HACCP, providing a comprehensive understanding of its systematic approach:
a. Conducting Hazard Analysis: Identifying potential biological, chemical, and physical hazards associated with each step of the food production process.
b. Determining Critical Control Points (CCPs): Identifying critical points in the process where control measures can be applied to prevent, eliminate, or reduce hazards to an acceptable level.
c. Establishing Critical Limits: Setting measurable criteria that define the maximum or minimum values to which control measures must be maintained at CCPs to ensure food safety.
d. Monitoring CCPs: Implementing procedures to regularly observe and record the control measures applied at CCPs to ensure they remain within established critical limits.
e. Implementing Corrective Actions: Establishing protocols to take immediate action when monitoring indicates that a CCP is not within its critical limits, aiming to prevent unsafe food from reaching consumers.
f. Verifying the System: Periodically evaluating the effectiveness of the HACCP system to ensure it is functioning correctly and providing the desired level of protection.
g. Establishing Documentation and Record-Keeping: Maintaining comprehensive records of all procedures, actions, and results to demonstrate the application and effectiveness of the HACCP system.
Benefits of HACCP:
This section focuses on the numerous advantages offered by implementing HACCP within the food industry:
a. Enhanced Consumer Protection: By systematically identifying and managing hazards, HACCP significantly reduces the risk of foodborne illnesses, protecting consumer health and well-being.
b. Regulatory Compliance: HACCP is a widely recognized and mandated approach in many countries, ensuring compliance with regulatory requirements and fostering a culture of food safety.
c. Improved Product Quality: Implementing HACCP promotes consistent adherence to quality standards, leading to improved product quality and customer satisfaction.
d. Cost Reduction:
Hazard analysis critical control point (haccp)Allwyn Vyas. G
Hazard analysis and critical control points or HACCP is a systematic preventive approach to food safety from biological, chemical, and physical hazards in production processes that can cause the finished product to be unsafe, and designs measurements to reduce these risks to a safe level.
A method known as 'current Good Manufacturing Practice (GMP) is used to guarantee that goods are consistently manufactured and monitored in accordance with quality standards. Good Manufacturing Practices is intended to reduce any production-related hazards associated with pharmaceuticals that cannot be avoided via evaluating the finished product.
Why is GMP crucial?
In addition to being a health risk, low-quality medications cost both governments and individual customers money.
Medicines of poor quality can harm one's health.
Unintentionally added harmful chemicals may be found in low-quality medications.
A medication won't have the desired therapeutic outcome if it contains little to no of the advertised component.
Describe GMP.
A method known as 'current Good Manufacturing Practice (GMP) is used to guarantee that goods are consistently manufactured and monitored in accordance with quality standards. It is intended to reduce any production-related hazards associated with pharmaceuticals that cannot be avoided via evaluating the finished product. The primary dangers include unanticipated product contamination, which can harm health or even result in death; inaccurate labelling on containers, which might result in patients receiving the wrong medication; and an inadequate or excessive amount of active component, which can lead to ineffective therapy or negative consequences. GMP covers every aspect of production, including raw materials, space, and tools, as well as employee training and personal hygiene. Every process that might have an impact on the final product's quality requires specific, written procedures. To be there
If there is a quality control laboratory, is GMP still required?
Yes. Quality cannot be tested into a product after it has been produced; it must be built in during the manufacturing process. GMP guards against mistakes that can't be caught by final product quality control. Without GMP, it is impossible to ensure that each individual dose of a medication is of the same calibre as the sample doses examined in a laboratory.
Can businesses afford to adopt GMP?
Yes. Making cheap items does not result in cost savings. In the long run, fixing mistakes after they have been committed is more expensive than avoiding them in the first place. GMP aims to stop mistakes from occurring. Implementing GMP is a financial investment in premium drugs. In addition to helping the pharmaceutical business and healthcare professionals, this will enhance the health of the individual patient and the community. Poor quality pharmaceutical production and distribution damage the reputation of the company, the public health system, and private health care.
WHO strives to improve GMP
WHO GMP regulations are accessible online. Please get in touch with the WHO representative in your nation, your WHO regional office, or WHO headquarters in Geneva if you need additional information.
In addition, an impartial, independent body should periodically carry out a thorough verification of the HACCP system. These authority may reside inside or outside the food operation. In addition to an on-site inspection of all flow diagrams and the pertinent data from the plan’s execution, this should include a technical evaluation of the hazard analysis and each component of the HACCP plan
To guarantee that the identified risks are avoided, handled, or reduced to tolerable levels, each CCP will comprise one or more control measures. Each control measure has one or more crucial limitations that go along with it. Temperature, time, physical dimensions, humidity, moisture content, water activity (aw), and others may all serve as critical constraints.
The preparation of beef patties is one instance (Appendix B). The procedure need to be planned to guarantee the creation of a secure product. Enteric infections, such as salmonellae and verotoxigenic E. coli O157:H7, were deemed to be the most serious biological dangers for cooked pork patties. Additionally, it is during the cooking process that control may be used to lower the intestinal pathogens to a tolerable level. It is essential to have accurate knowledge of the anticipated concentration of pathogens in the raw patties, their heat tolerance, the variables influencing how well they heat up, and the section of the patty which warms the slowest in order to guarantee that an appropriate level is routinely obtained.
In an era where food safety is of paramount importance, HACCP has emerged as a systematic and preventive approach to identifying and managing potential hazards in food production processes. This presentation aims to shed light on the fundamental principles of HACCP, its benefits, and its significance in ensuring the safety of our food supply.
Definition and Background:
We begin by defining HACCP as an internationally recognized food safety management system designed to identify, evaluate, and control hazards that may pose risks to the safety of food products. It originated in the 1960s, developed by the Pillsbury Company in collaboration with NASA, with the primary objective of ensuring safe food for astronauts. Since then, HACCP has been widely adopted and applied across various sectors of the food industry.
Principles of HACCP:
Next, we delve into the seven core principles of HACCP, providing a comprehensive understanding of its systematic approach:
a. Conducting Hazard Analysis: Identifying potential biological, chemical, and physical hazards associated with each step of the food production process.
b. Determining Critical Control Points (CCPs): Identifying critical points in the process where control measures can be applied to prevent, eliminate, or reduce hazards to an acceptable level.
c. Establishing Critical Limits: Setting measurable criteria that define the maximum or minimum values to which control measures must be maintained at CCPs to ensure food safety.
d. Monitoring CCPs: Implementing procedures to regularly observe and record the control measures applied at CCPs to ensure they remain within established critical limits.
e. Implementing Corrective Actions: Establishing protocols to take immediate action when monitoring indicates that a CCP is not within its critical limits, aiming to prevent unsafe food from reaching consumers.
f. Verifying the System: Periodically evaluating the effectiveness of the HACCP system to ensure it is functioning correctly and providing the desired level of protection.
g. Establishing Documentation and Record-Keeping: Maintaining comprehensive records of all procedures, actions, and results to demonstrate the application and effectiveness of the HACCP system.
Benefits of HACCP:
This section focuses on the numerous advantages offered by implementing HACCP within the food industry:
a. Enhanced Consumer Protection: By systematically identifying and managing hazards, HACCP significantly reduces the risk of foodborne illnesses, protecting consumer health and well-being.
b. Regulatory Compliance: HACCP is a widely recognized and mandated approach in many countries, ensuring compliance with regulatory requirements and fostering a culture of food safety.
c. Improved Product Quality: Implementing HACCP promotes consistent adherence to quality standards, leading to improved product quality and customer satisfaction.
d. Cost Reduction:
Hazard analysis critical control point (haccp)Allwyn Vyas. G
Hazard analysis and critical control points or HACCP is a systematic preventive approach to food safety from biological, chemical, and physical hazards in production processes that can cause the finished product to be unsafe, and designs measurements to reduce these risks to a safe level.
A method known as 'current Good Manufacturing Practice (GMP) is used to guarantee that goods are consistently manufactured and monitored in accordance with quality standards. Good Manufacturing Practices is intended to reduce any production-related hazards associated with pharmaceuticals that cannot be avoided via evaluating the finished product.
Why is GMP crucial?
In addition to being a health risk, low-quality medications cost both governments and individual customers money.
Medicines of poor quality can harm one's health.
Unintentionally added harmful chemicals may be found in low-quality medications.
A medication won't have the desired therapeutic outcome if it contains little to no of the advertised component.
Describe GMP.
A method known as 'current Good Manufacturing Practice (GMP) is used to guarantee that goods are consistently manufactured and monitored in accordance with quality standards. It is intended to reduce any production-related hazards associated with pharmaceuticals that cannot be avoided via evaluating the finished product. The primary dangers include unanticipated product contamination, which can harm health or even result in death; inaccurate labelling on containers, which might result in patients receiving the wrong medication; and an inadequate or excessive amount of active component, which can lead to ineffective therapy or negative consequences. GMP covers every aspect of production, including raw materials, space, and tools, as well as employee training and personal hygiene. Every process that might have an impact on the final product's quality requires specific, written procedures. To be there
If there is a quality control laboratory, is GMP still required?
Yes. Quality cannot be tested into a product after it has been produced; it must be built in during the manufacturing process. GMP guards against mistakes that can't be caught by final product quality control. Without GMP, it is impossible to ensure that each individual dose of a medication is of the same calibre as the sample doses examined in a laboratory.
Can businesses afford to adopt GMP?
Yes. Making cheap items does not result in cost savings. In the long run, fixing mistakes after they have been committed is more expensive than avoiding them in the first place. GMP aims to stop mistakes from occurring. Implementing GMP is a financial investment in premium drugs. In addition to helping the pharmaceutical business and healthcare professionals, this will enhance the health of the individual patient and the community. Poor quality pharmaceutical production and distribution damage the reputation of the company, the public health system, and private health care.
WHO strives to improve GMP
WHO GMP regulations are accessible online. Please get in touch with the WHO representative in your nation, your WHO regional office, or WHO headquarters in Geneva if you need additional information.
In addition, an impartial, independent body should periodically carry out a thorough verification of the HACCP system. These authority may reside inside or outside the food operation. In addition to an on-site inspection of all flow diagrams and the pertinent data from the plan’s execution, this should include a technical evaluation of the hazard analysis and each component of the HACCP plan
To guarantee that the identified risks are avoided, handled, or reduced to tolerable levels, each CCP will comprise one or more control measures. Each control measure has one or more crucial limitations that go along with it. Temperature, time, physical dimensions, humidity, moisture content, water activity (aw), and others may all serve as critical constraints.
The preparation of beef patties is one instance (Appendix B). The procedure need to be planned to guarantee the creation of a secure product. Enteric infections, such as salmonellae and verotoxigenic E. coli O157:H7, were deemed to be the most serious biological dangers for cooked pork patties. Additionally, it is during the cooking process that control may be used to lower the intestinal pathogens to a tolerable level. It is essential to have accurate knowledge of the anticipated concentration of pathogens in the raw patties, their heat tolerance, the variables influencing how well they heat up, and the section of the patty which warms the slowest in order to guarantee that an appropriate level is routinely obtained.
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2. Food Safety Management Systems
10-2
Food safety management system:
Group of practices and procedures intended to prevent
foodborne illness
Actively controls risks and hazards throughout the flow of food
3. Food Safety Management Systems
These are the foundation of a food safety management
system:
Food safety training program
Quality control and
assurance program
Supplier selection and
specification program
Personal hygiene program
10-3
4. Food Safety Management Systems
These are the foundation of a food safety management
system:
Standard operating
procedures (SOPs)
Pest control program
Facility design and
equipment
maintenance program
Cleaning and
sanitation program
10-4
5. Active Managerial Control
10-5
Focuses on controlling the five most common risk
factors for foodborne illness:
1. Purchasing food from unsafe sources
2. Failing to cook food adequately
3. Holding food at incorrect temperatures
4. Using contaminated equipment
5. Practicing poor personal hygiene
6. Active Managerial Control
10-6
There are many ways to achieve active managerial
control in the operation:
Training programs
Manager supervision
Incorporation of standard operating procedures (SOPs)
HACCP
These are critical to the success of active managerial
control:
Monitoring critical activities in the operation
Taking the necessary corrective action when required
Verifying that the actions taken control the risks factors
7. The FDA’s Public Health Interventions
The FDA provides recommendations for
controlling the common risk factors for
foodborne illness:
Demonstration of knowledge
Staff health controls
Controlling hands as a vehicle of
contamination
Time and temperature parameters for
controlling pathogens
Consumer advisories
10-7
8. HACCP
10-8
The HACCP approach:
HACCP is based on identifying significant biological, chemical,
or physical hazards at specific points within a product’s flow
through an operation
Once identified, hazards can be prevented, eliminated, or
reduced to safe levels
9. HACCP
10-9
To be effective, a HACCP system must be based on a
written plan:
It must be specific to each facility’s menu,
customers, equipment, processes, and operations
A plan that works for one operation may not work for another
10. HACCP
10-10
The seven HACCP principles:
1. Conduct a hazard analysis
2. Determine critical control points (CCPs)
3. Establish critical limits
4. Establish monitoring procedures
5. Identify corrective actions
6. Verify that the system works
7. Establish procedures for record keeping and documentation
11. HACCP
Principle 1: Conduct a hazard analysis
Identify potential hazards in the food served by looking at how it
is processed
Identify TCS food items and determine where hazards are likely
to occur for each one; look for biological, chemical, and physical
contaminants
10-11
12. HACCP
Principle 2: Determine critical control
points (CCPs)
Find points in the process where identified
hazards can be prevented, eliminated, or
reduced to safe levels—these are the CCPs
Depending on the process, there may be
more than one CCP
10-12
13. HACCP
Principle 3: Establish critical limits
For each CCP, establish minimum or
maximum limits
These limits must be met to
o Prevent or eliminate the hazard
o Reduce it to a safe level
Critical
Limit
10-13
14. HACCP
Principle 4: Establish monitoring
procedures
Determine the best way to check critical limits
o Make sure they are consistently met
Identify who will monitor them and how often
10-14
15. HACCP
Principle 5: Identify corrective actions
Identify steps that must be taken when a
critical limit is not met
Determine these steps in advance
10-15
16. HACCP
Principle 6: Verify that the system works
Determine if the plan is working as intended
Evaluate the plan on a regular basis using
o Monitoring charts
o Records
o Hazard analysis
Determine if your plan prevents, reduces, or
eliminates identified hazards
10-16
17. HACCP
Principle 7: Establish procedures for record keeping and
documentation
Keep records for these actions:
Monitoring activities
Corrective actions
Validating equipment (checking for good
working condition)
Working with suppliers (invoices, specifications, etc.)
10-17
18. HACCP
10-18
These specialized processing methods require a
variance and may require a HACCP plan:
Smoking food as a method to preserve it (but not to
enhance flavor)
Using food additives or components such as vinegar to
preserve or alter food so it no longer requires time and
temperature control for safety
Curing food
Custom-processing animals
19. HACCP
10-19
These specialized processing methods require a
variance and may require a HACCP plan:
Packaging food using ROP methods including
o MAP
o Vacuum-packed
o Sous vide
Treating (e.g. pasteurizing) juice on-site and packaging it for
later sale
Sprouting seeds or beans
20. Crisis Management
To build a crisis-management program:
Create a crisis-management team
Prepare for different types of crises
Create a written plan tailored to your
operation
Test your plan
10-20
21. Crisis Management
To prepare for a crisis:
Create a crisis-management team
Create an emergency-contact list
Develop a crisis-communication plan
10-21
22. Crisis Management
To prepare for a foodborne-illness outbreak:
Develop a food safety program
Train staff on food safety policies and procedures
Create a foodborne illness incident
report form
o Get legal guidance when developing it
o Train staff to use it
10-22
23. Crisis Management
The foodborne illness incident report form
should document the following:
What and when the customer ate at the
operation
When the customer first got sick, what the
symptoms where, and how long they were
experienced
When and where the customer sought medical
attention
What other food was eaten by the customer
10-23
24. Crisis Management
10-24
When responding to a crisis:
Work with the media
Communicate directly with your key audiences (customers,
stockholders, the community)
Fix the problem and then communicate what you have done
25. Crisis Management
When responding to a foodborne-
illness outbreak:
Take the complaint seriously and express
concern
Complete an incident report form
Contact your crisis-management team and
the local health department
Follow your crisis-communication plan
10-25
26. Take the complaint seriously and
express concern
Don’t admit responsibility
Ask for general contact information
Complete the foodborne-illness
incident report form
10-26
A customer calls to
report a foodborne
illness
Responding to a Foodborne-Illness Outbreak
If: Then:
27. Contact the crisis-management
team
Identify common food items to
determine the potential source of
the complaint
Contact the regulatory authority to
assist with the investigation if an
outbreak is suspected
10-27
There are similar
customer complaints of
foodborne illness
Responding to a Foodborne-Illness Outbreak
If: Then:
28. Responding to a Foodborne-Illness Outbreak
10-28
If
:
Then:
Set aside the suspected product
and identify it to prevent further sale
Label the product with a “Do Not
Use” and “Do Not Discard” label
Log information about the product
including a description, product
date, and lot number
If possible, obtain samples of the
suspect food from the customer
The suspected food is
still in the operation
29. Responding to a Foodborne-Illness Outbreak
10-29
Then:
Maintain a list of food handlers
scheduled at the time of the
suspected contamination
Interview them about their health
status
Exclude the suspected staff member
from the operation following
requirements
If:
The suspected
outbreak is caused by
a sick staff member
30. Responding to a Foodborne-Illness Outbreak
10-30
Cooperate with the regulatory
authority to resolve the crisis
Provide appropriate documentation
including temperature logs, HACCP
documents, staff files, etc.
If: Then:
The regulatory
authority confirms your
operation is the source
of the outbreak
31. Crisis Management
10-31
To recover from a foodborne-Illness outbreak:
Investigate to find the cause of the outbreak
Work with the regulatory authority to resolve issues
Throw out all suspected food
Clean and sanitize all areas of the operation
Establish new procedures or revise existing ones
based on the investigation results
Develop a plan to reassure customers that the food served in
your operation is safe