Food Safety Systems Management Food Safety Systems Management GS TS BS Lê Hoàng Ninh Hazard Analysis Critical Control Point Cách tiếp cận hệ thống để xác định, đánh giá và kiểm soát các mối nguy có[.]
Trang 1Food Safety Systems
Management
GS TS BS Lê Hoàng Ninh
Trang 2Hazard Analysis Critical
Control Point
Cách tiếp cận hệ thống để xác định, đánh giá
và kiểm soát các mối nguy có ý nghĩa làm
mất an toàn thực phẩm
Risk Assessment and Management tool not
unlike a FMEA (Failure Modes Effects
Analysis)
Trang 3NỀN TẢNG HACCP
-Prerequisite Programs
HACCP
Raw Materials Control
Sanitation
Facility Design And Control
Equipment Design And Maintenance
Pest Control
Traceability
And Recall Employee Training
Trang 4 Phải tương thích và có hiệu quả
Phải được giám sát, theo dõi (requires
documentation and records) – Internal Audit.
Các sai sót cứ lập lại rõ ràng không ủng hộ cho
HACCP.
Trang 5Raw Materials Control
Trang 6Kiểm soát chất liệu thô
(Raw Materials Control)
Supplier licensing and registration must meet state and federal requirements (e.g FDA Registration for Bioterrorism Act of 2002)
Material Guarantee and Supplier Certificate of
Insurance
Supplier Food Safety Audit (second or third party)
Raw Material Specifications - includes capability
assessment on critical parameters
Certificate of Analysis – on critical to quality
parameters
Supplier HACCP Risk Assessment
Handling / Shipping Requirements
Trang 7Kiểm soát chất liệu thô
(Raw Materials Control
Phải có hồ sơ thanh / kiểm tra các công cụ phương tiện tiếp nhận các nguyên liệu thô
nầy (temperature, sanitation)
Vật liệu được kiểm tra phải có chứng nhận Materials inspected upon receipt Visual
inspection, grading, as your program has defined
Tồn trử phù hợp để đảm bảo chất lượng
(allergen segregation, temperature, protected, chemicals stored separately and secured, etc).
Trang 8Sanitation
Trang 9 Effective cleaning procedures for equipment and
facility.
Documented – SSOP (Sanitation Standard Operating Procedures)
Defined frequency
Chemicals approved for use in food facilities.
Records – concentrations, times, temperatures.
Sanitation monitoring – visual inspections, chemical or microbiological testing.
Corrective actions for deficiencies.
Trang 10Employee Training
Trang 11 Records of training required.
Hygienic Practices
Disease Control
Cleanliness – outer garments, hand-washing, unsecured jewelry and other objects, use of gloves, hair and beard nets, eating, drinking, tobacco use, nail polish, etc.
Manufacturing Controls
Traffic flow to prevent cross contamination
Ingredient / product handling to protect product
Control measures (pH, cook time / temp, moisture, etc)
Scheduling sequential runs to prevent cross contamination (as for allergens)
Food Defense
Trang 12Thiết kế và kiểm soát cơ sở (Facility Design and Control)
Trang 13Thiết kế và kiểm sóat cơ sở
Facility Design and Control
Mặt đất
Eliminate pest harborage areas
Properly grade roads, yards, parking lots
Trang 14Thiết kế và kiểm soát cơ sở
Facility Design and Control
Sàn , tường, trần nhà Floors, walls and ceilings
cleaned and in good repair
Prevent condensate
Ánh sáng đủ Adequate lighting
Thông khí phù hợp Adequate ventilation
Chất lượng nước Water Quality (potable, steam, ice, reclaimed water, cooling water, backflow prevention)
Nghỉ dưỡng nhân viên / nhà vệ sinh
Kiểm soát chất thải
Giám sát theo dõi môi trường
Trang 15Equipment
Design and Maintenance
Trang 16Equipment
Design and Maintenance
Designed and of materials and workmanship
as to be adequately cleanable – meets
standards (e.g 3A Sanitary Standards)
Installed with adequate space to allow for
proper cleaning and maintenance and to
prevent cross contamination
Properly maintained (records)
Trang 17Pest Control
Trang 18 Prevention is key (design, maintenance and sanitation)
Rodent control
Insect control
Bird / Bat Control
Trang 19Traceability
and Product Recovery
Trang 20Traceability
and Product Recovery
Documented program with written procedures to
meet federal requirements
Program should include
Product Identification / Lot coding
Finished product distribution records retained beyond shelf life of product
Responsible individuals and their roles
Identification of Key Contacts – Internal, supplier customer
Mock Recovery Program
One step forward, one step back
Trang 21Prerequisite programs
are in place
Let’s talk HACCP
Trang 22Steps to
HACCP Implementation
Assemble the HACCP Team
Describe the food and its distribution
Describe the intended use and consumers of the food
Develop a flow diagram which describes the process
Verify the Flow Diagram
Trang 23Multidisciplinary HACCP Team
Trang 24Describe the Food /
Distribution: Cheddar Cheese
Formal Product name: Cheddar Cheese
Food Safety Characteristics: pH (4.9 to 5.4)
Packaging type: 42# Block, Vacuum sealed in ploy bag and stored in corrugated box
Length of shelf life/storage temperature: 3-12
months when stored below 45°F
Where it will be sold: Food Manufacturer
Intended Consumers: Consumers of all ages
Labeling instructions: Keep Refrigerated
Intended use: Ready to eat product May be used
as ingredient May be further processed into
chunks or shredded.
Trang 25Develop a Flow Diagram
Trang 26Verify the Flow Diagram
HACCP Team should perform an on-site
review of the operation to verify the accuracy and completeness of the flow diagram
Take the diagram out to the production floor and walk through the steps
Review periodically, modify and update as
necessary (annual review or when change to process occurs)
Trang 271 - Conduct a Hazard Analysis
Identify hazards at each processing step and
for each ingredient and material used.
Biological – such as pathogen
Chemical – such as toxin
Physical - such as glass
Evaluate hazards to determine severity and
likelihood to occur
The hazard evaluation provides a basis for
determining control measures such as CCP’s
Trang 282 - Determine Critical Control
Trang 293 – Establish Critical Limits
A critical limit must be scientifically based and is a maximum and / or minimum value
to which a biological, chemical or physical parameter must be controlled at a CCP to prevent, eliminate or reduce the food
safety hazard to an acceptable level.
Examples: Temperature, time, Water
Activity, pH, safe tolerance level for drug residues
Trang 304 – Establish Monitoring
Procedures
Monitoring is a planned sequence of
observations or measurements used to
assess whether a CCP is under control
Monitoring should produce an accurate
record for use in verification
Where there is loss of control (a CCP limit is exceeded) there must be documented
corrective action
Trang 31 Continuous is desirable (recording chart) but where not possible, frequency for monitoring must be established
Responsibility for monitoring must be
assigned - Position title / work station
Trang 325 - Establish Corrective
Actions
Corrective actions are procedures to be followed when a deviation occurs.
Corrective actions must be specific.
Halt production of product
Isolate the affected product
Return the process to control
Determine the disposition of the product
Records must be kept for a reasonable
period after the shelf life of the product
Trang 336 _ Establish Verification
Procedures
Establish procedures to verify that the system is working properly.
Might include calibration and testing of
monitoring equipment, demonstration of system performance, documented record review
Trang 34 Verification and Validation Records
Records to show changes to the HACCP Plan
Trang 35Consider our example
Trang 36Identify hazard at each step and for each material
Raw Milk Receiving
Raw Milk,
Water
Trang 371 – Conduct Hazards Analysis
Identify the hazards for each step of the process: Raw milk / receiving
Identify the type of hazard: chemical,
Trang 38Determine severity of each hazard
and likelihood of occurrence
Severity: Enteric pathogens such as E coli
0157H7 and Salmonella cause severe health effects including death among children and elderly
Likelihood to occur: Likely that they will
occur in raw milk supply
Using this information, determine if this
potential hazard is to be addressed in the
HACCP Plan
Trang 39Hazards Analysis (severity)
Is the hazard identified at this step severe
and of sufficient likelihood of occurrence to warrant it’s control? If Yes, go to next
question
If no, identify the prerequisite program or
procedure step, which reduces the likelihood
or severity of the hazard to ensure that
control at this step is not necessary
Trang 40Hazards Analysis (control)
Does a control measure exist at this step to prevent, reduce or eliminate the likely
occurrence of the hazard to an acceptable level?
If yes, this step is a CCP
If no, identify where control exists
(Pasteurization Step – This step is a CCP)
Trang 41Hazards Analysis (justify)
Justification - Research or Reference
Document that gives credence to your
assumptions Pasteurized Milk Ordinance,
2003 Revision, WDATCP 80.48
Trang 422 - Determine Critical Control Points
Trang 433 - Establish Critical Limits
Critical Limits
HTST Limits for raw milk pasteurization are defined in the PMO – minimum 161˚F / 15 seconds
Trang 455 - Establish Corrective Actions
When minimum time or temperature requirement
is not met, product automatically diverts to back
to the balance tank prior to the HTST
Pasteurizer Forward flow is prevented
Product diversion must be indicated on
Pasteurizer Recording chart These instances
should be carefully reviewed by Licensed
Pasteurizer Operator
Trang 466 _ Establish Verification
Procedures
after sanitation and before product (Cut In / Cut Out) and recorded on the continuous chart Charts verified
Licensed Pasteurizer Operator.
Pasteurizer / time (maximum allowable flow for specified distance) and temperature All controls are sealed
Records are retained by facility and state.
reviewed by Licensed Pasteurizer Operator.
Trang 477 – Establish Records
Pasteurizer Charts
Seal Check Record
WDA Pasteurizer Time / Seal Record
Other Equipment Calibration and testing records
Trang 48Identify CCP on Flowchart
Trang 49HACCP Description Chart
Trang 50 International Dairy Foods Association –
HACCP Plant Manual, 2007 Edition
Pasteurized Milk Ordinance, 2003 Revision
WDATCP Chapters 60 and 80
USDA-FSIS HACCP Website