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Chemical Bulletin of “Politehnica” University of Timisoara, ROMANIA
Series of Chemistry and Environmental Engineering
Chem. Bull. "POLITEHNICA" Univ. (Timisoara) Volume 56(70), 1, 2011
47
Quality Control of Pastry Products using the HACCP Method
M. Panfiloiu*
, M.C. Cara**
, D.M. Perju***
and G.A. Dumitrel***
*
S.C. Antarctica S.R.L. Timisoara, Sanmihaiul Roman Nr.526A, Romania, mirabelapanfiloiu@yahoo.com
**
Sanitary-Veterinary and Food Safety Directorate of Timis, Surorile Martir Caceu 4, Timisoara, Romania
***
POLITEHNICA University of Timisoara, Industrial Chemistry and Environmental Engineering Faculty, 300006, 2
Victoriei Square, Timisoara Romania, Phone:+40-256-403073; Fax:+40-256-403060
Abstract: HACCP is a procedure that companies have to apply in order to protect the quality of food products. The
purpose of this paper is to describe the critical points in which hazard can come to light in the production process, the
evaluation and the measures applied to prevent and control these critical points. This method is applied to all the
technological processes in order to obtain the pastry products without yeasts.
Keywords: pastry products, hazard analysis, critical control points.
1. Introduction
HACCP is an acronym for “Hazard Analysis and
Critical Control Points”. It is a preventive method used for
increasing the safety of food, cosmetics and drugs. The
method appeared in 1971 in the U.S.A.
The European Community has promoted since 1983
introduction of HACCP principles in its legislation. In the
EU Council Directives on food hygiene HACCP is a
concept as well as a method of operation, applied to all
phases of food production. The purpose of these directives
is to encourage food manufacturers and retailers in the
application of HACCP in their own companies. In the UK,
in September 1995 a mandatory application of HACCP has
been instituted in all links of the food chain [1].
HACCP is a scientific system of self control of the
manufacturing process, which has been extensively used in
food production to prevent problems that may occur, using
the critical control points (CCP) in manufacturing process,
where the risk can be controlled, reduced or eliminated. A
company must have a real system to meet requirements and
prevent spoilage of products. It is a system that controls the
relevant hazards to food safety, through Critical Control
Points (CCP). A CCP is defined as a point, step, or
procedure in a food manufacturing process at which:
- control that is essential to prevent or eliminate a
food safety hazard or reduce it to an acceptable level can be
applied; and where,
- later processing steps won’t correct these safety
problems [2].
If one of the parameters of the CCP are out of control
it is possible to reach the compromise of food safety.
Unlike Critical Control Point, Control Point (CP) is any
step in the process at which biological, chemical, or
physical risks or hazards can be controlled, and usually is
related to quality or production issues and not to product
safety, unless the control point supports a CCP.
The hazard is any physical, chemical, biological agent
or body, which, if present in the food in the moment of
consumption, has the capacity to affect the innocuity or the
hygienic quality of the product.
A critical limit is defined as 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 to an acceptable level, the occure of a
food safety hazard. A critical limit is used to distinguish
between safe and unsafe operating condition at a CCP.
By monitoring CCP, the elimination of the risk is
ensured or the risk is reduced by keeping it at levels below
the critical limit. The monitoring of CCP means
observation and planned measurement of risk from that
critical control point. It is achieved through: inspection,
sensory assessment, physical records, chemical analysis
and microbiological analysis. Following an international
statistics, it appeared that the ratio of chemical and
biological hazards is 1/100 000. The laws of our country
require that mandatory implementation of HACCP system,
not its certification.
Some benefits of implementation or certification of
the system are:
- A quality system that ensures food safety meaning
that the food will not affect consumers if food is prepared
or consumed as indicated;
- Is the guarantee for the production and trade of
safe food, being transparent, both for official inspection,
and consumers;
- Is a quality system "urged" by retailers (who are
first in contact with customers and stakeholders to market
safe products);
- Is a system that minimizes risk over the
technological process [3].
HACCP implementation is related to determining in
advance the rules of good practice on the following:
construction, machines location, technological process,
personnel, cleaning and disinfection, pest control, raw and
auxiliary materials used, including water, product
traceability, transport.
HACCP team should be multidisciplinary and include
a motivated member of the executive management who is
Chem. Bull. "POLITEHNICA" Univ. (Timisoara) Volume 56(70), 1, 2011
48
able to provide necessary financing and general motivation
of the company to ensure successful implementation of
HACCP. HACCP team will also need a well educated
person who will lead the implementation of HACCP.
The team should include multidisciplinary specialists:
who understand biological, chemical and physical hazards
associated with a particular group of products, who are
responsable or involved in production / manufacturing of
products, who have experience and practical knowledge of
hygiene, and working process and function of the
equipment operating within the organization, as well as
other specialists with appropriate knowledge in
microbiology, hygiene and food processing technology [5].
Optimally, a multidisciplinary team will be built
within the organization. But which lacks the necessary
experience, the team should be assisted by qualified
specialists/ experts to help them resolve difficulties,
including risk analysis, control and determination of the
critical control points. Experts can be from the commercial
and industrial associations, independent experts and
regulatory authorities.
HACCP plans are developed by the HACCP team and
approved by the General Manager of the Company.
Distribution of documents is based on the distribution list,
so that at any moment the workplace where they were
broadcast is known.
Along with the distribution of documents available,
obsolete documents are promptly removed from all points
of distribution, by the concern of the elaboration unit. After
withdrawal invalid documents are destroyed or identified
by writing "invalid". Change documents may be
determined by revising the organization and functioning of
society, reference documents (regulations, rules, laws, etc.)
and applications employees / customers / suppliers /
external organizations.
Because the information contained in the records must
be complete and easy accessible, forms are used. That
forms offer directions regarding the data that has to be
recorded.
By their format they provide indications of data to be
recorded. Encoding of the forms is made by Quality Officer
in accordance with regulations: “The development and
codification of procedures, work instructions and HACCP
plans”. The preservation of the documents is for a specified
period of time.
Verification of the HACCP plan will be made
quarterly. Tests and other evaluation methods will be
applied in order to determine if the system is effective [6].
Tests will be applied on:
The production process
- Analysis of process deviations that occur
- Analysis of corrective measures taken
2. Conditions of production
- hygiene plan testing
- maintenance plan testing
- testing the method of recording and handling
complaints from customers
- Testing the training method
3. Final products - a quality control of the product is
made by sampling the final product.
Plan review will be made annually or if changes occur
in conditions or methods of operation:
- Changing raw materials, ingredients or primary
packaging
- Acquiring new equipment or other changes in
processing conditions
- Changes in the technological flow
- Changes in legislation
- Changing equipment
The present paper aims at identifying and monitoring
potential risks in the process of cheese pastry, and
implementation of corrective actions in order to restore
critical control points within acceptable limits.
2. Experimental
The product considered in this paper is a pastry
product made from dough without yeast, with a
homogeneous cheese-based filling. The product is
distributed frozen, roasting and selling being achieved at
the point of working partners [5]. Raw materials and
materials used in the manufacturing process are presented
in table 1.
TABLE 1. Raw materials and materials used in the manufacturing
process
Name of raw materials Quantity %
Meal 32.23
Water 27.84
Margarine for puffs 25
Cottage 15
Sour 3
Thickener 2.33
Milk replacer powder 1.15
Salt 0.87
Acidifying 0.58
Sugar 0.29
Dyes 1.36
In table 2 (Physicochemical characteristics) and 3
(Microbiological characteristics) are showed the
physicochemical and microbiological characteristics of the
studied frozen product [5].
TABLE 2. Physicochemical characteristics
Features Conditions of eligibility Verification methods
Content filler% 25-30 STAS 91/83
Fat content,% 30-35 STAS 91/83
Total salt,% 1-3 STAS 91/83
Humidity,% 40-45 STAS 91/83
TABLE 3. Microbiological characteristics
Features Verification methods Limits
Escherichia coli ISO 16649-2/2002 Absent
Salmonella SR EN ISO 6579/03 Absent
Stafilococus coagulazopositiv SR EN ISO 6888-1/2002 Absent
Packaging of the finished product is in printed
polyethylene bags and PVC boxes and the closure of the
bags is made by thermal closure. The storage is made by
freezing at least -18 ± 3°C, protected from external effects.
The transport is made with special vehicles so that the cold
chain is respected, and that no changes will occur [5].
Chem. Bull. "POLITEHNICA" Univ. (Timisoara) Volume 56(70), 1, 2011
49
3. Results and Discussion
Potential risks were identified in the process of cheese
puff pastry. Then the risks have been evaluated using the
criteria resulted from the severity and frequency of risk
occurrence.
Gravity is the consequences suffered by a consumer
from exposure to a contaminant and is divided as follows:
-High (3 points) - fatal consequences, serious illness,
incurable damage that occurs either immediately or after a
longer period
- Media (2 points) - substantial damage and / or
illnesses
- Small (1 point) and minor injuries or illness, minor
effects or no effects at all.
Frequency is the probability to have a contaminant in
the final product upon consumption. Probability is
determined by measurements or observations during certain
specific situations arising during the manufacturing
process.
They are classified as:
- Small (1 point) - virtually impossible to produce or
improbable
- Media (2 points) - can occur, they happen to occur
- High (3 points) – it occurs systematically.
Stability risk class was made taking into account the
four possible levels: level one - no measure of control
(f × g = 1), level 2 - without control measures, but in risk
analysis you take into account this risk (f × g = 2; 3), level
3 - general control measures for possible control points
(f × g = 4), level 4 - specific control measures to eliminate
or reduce risk to acceptable levels (f × g = 6;9). Control
measures were established for each risk.
HACCP team has determined the critical control
points through the “Decision tree method”, analyzing risks
of 2,3,4 degree [7].
Figure 1 “A decision tree” is presented to identify
critical control points.
Figure 1. Decisional tree
The critical control points for pastry without yeast have
been determined at all stages of the technological flow
(figure 2).
Figure 2. Technological flow chart
Table 4 presents only those stages of the production
process, which will be monitored to eliminate non-
compliance. For each critical control point acceptable
limits were set, taking into account the existing regulatory
requirements and manufacturing technology. When critical
limits of critical control points have been reached or are
about to be reached, the product is identified and isolated
and will be treated as non-compliant product.
To restore the process within the default parameters
of the manufacturing technology and in order to restore the
critical control point within the allowed limits, corrective
actions are established following the steps:
1. Analysis of identified problems is made in order to
determine their causes, for taking correct decisions for
corrective actions. The analysis of deficiencies occurred is
made by the HACCP team. In its analysis, the main
problem is breakdown in partial problems and a hierarchy
of importance is established. Once the individual influences
of each second problem on the main problem is established,
the causes of the second problem are identified.
2. The establishment of the causes of the existing
problems is made after the analysis performed by the
HACCP team.
Chem. Bull. "POLITEHNICA" Univ. (Timisoara) Volume 56(70), 1, 2011
50
Possible causes of identified or potential problems
are:
- Inadequate or nonexistent procedures and
instructions
- Failure of procedures or instructions
- Lack of control of the processes
- Lack of appropriate training
- Improper working environment
- Financial and human resources inadequate or
insufficient.
3. The establishment and the implementation of
corrective actions is made in order to remove causes of the
existing non-compliances.
HACCP team established methods for monitoring
critical control points (CCP) and the correct actions
required to be applied when exceeding the critical limits
established.
In Table 5 methods are presented through which are
made: monitoring, frequency and corrections to be applied
to eliminate risk.
In order to restore critical control points within the
allowed limits, responsible have been designated for
monitoring the steps taken into discussion and other
responsible which will deal with the implementation of
corrective actions. Recordings will be made according to a
pre-verification program.
In Table 6 appointed responsible are presented, and
also the records that have to be made regarding the
applicability of corrective actions.
TABLE 4. Critical control points
“Decision tree” questions
No. Stage of technological process Risk Risk class
Q1 Q2 Q3 Q4 CCP
1. Screening / dosing flour F-foreign body 4 YES YES - - YES
2. Freezer M–microbiological development 3 YES NO YES NO YES
3. Packaging / weighing / metal detection F-foreign body 4 YES YES - - YES
4. Cold storage M– microbiological development 3 YES NO YES NO YES
5. Unloading cars at the premises and the partners M–microbiological development 3 YES NO YES NO YES
TABLE 5. Monitoring, frequency and corrections
Critical value MonitoringStage of technological
process Risk Parameter Allowable limit Method Frequent Corrective actions
Screening / dosing flour
F foreign body Absent
Cleaning and
checking sites
Weekly
Replacement sites
Freezer M
Core
temperature
of frozen
product
Maximum
- 13°C
Thermometer
measurement
kernel
-freezer shock:each
trolley;
-tunnel freezer: each
kneading
-Declaring non-compliant
product
- Prohibition of leaving the
cold store frozen products 72
hours min
Packaging / weighing /
metal detection
F
Metal
objects
Feros ∅2,0 mm
Neferos ∅2,0
mm
steel ∅3,0 mm
Metal detection,
verification
standards
Each package of
frozen, from 3 to 3:00
hour random
download
Declaring non-compliant
product
Cold storage at
headquarters and in the
premises of
M
Storage
temperature + 18±3°C
Monitoring
parameters storage
Standing on the
viewing display,
scoring 6 times per day
-Technical department store
closing
-Announcement, application
services provider of cold air
service,
- Declaring non-compliant
product
Unloading cars at the
premises and the
partners
M
Core
temperature
of frozen
product
Maximum
- 13°C
Thermometer
measurement
kernel
Every download
-Declaring non-compliant
product;
-Prohibition of leaving the
cold store frozen products 72
hours min
Chem. Bull. "POLITEHNICA" Univ. (Timisoara) Volume 56(70), 1, 2011
51
TABLE 6. Responsible for implementing corrective actions and for monitoring
Stage of
technological process
Responsible monitoring Responsible for implementing
corrective actions
Recordings
Screening / dosing
flour
Appointed Technical
Department
Head of technical department
"Weekly checks Schedule"
Freezer Packer
-Department quality-control product
-Commission analysis of non-
compliance
"Application of shock freezing"
"Application of freezing tunnel"
"Report of noncompliance"
Packaging / weighing
/ metal detection
- Metal-detector
- Chief packing, respectively
-Department quality-control
product
-Department quality-control product
"Application of product verification
parameters"
"Report of non-compliance items"
Cold storage at
headquarters and in
the premises of
Chiefs and heads of
exchange deposits
-Chief Deposit
- Technical Department
- Department-product quality-control
"Track temperatures in frozen food
store" - headquarters
"Table for the notation temperatures"
work-points
Store bosses at the premises
- Commission of Analysis of non-
compliance
- Heads of deposits
Receiving frozen-Register
-Report of noncompliance
Unloading cars at the
premises and the
partners
Drive-in partners
Transport logistics department
Transport bosses
"Centralized route"
"Report of non-compliance items"
4. Conclusions
HACCP examines the way of the development of
food production, the distribution, the evaluation of the risk
points, physically, chemically and microbiologically and
elaborates the ways to prevent hazards and the ways to
reduce risks.
Food Safety System - HACCP works by rules of good
hygiene and manufacturing practices, procedures and
instructions, appropriate training, discipline and
conscientious, good communication, accurate and complete
registration system and monitoring the CCP[4].
System efficiency can be proven by a safe finished
product on which microbiological and physicochemical
analysis do not indicate dangerous contaminants outside
the established maximum limits, no complaints, no major
deviations in the CCP, increased product market request
and little corrective action.
Maintaining the system of frozen food safety
operational, is assured by providing a plan of main actions
of the scheme. The main actions related to maintaining the
HACCP system are presented in table no 7.
Communication is an important factor in the smooth
implementation and operation of the HACCP system, as
this ensures a continuous link between all departments
involved in the action and also a good connection between
the departments and the HACCP team.
HACCP programs are necessary as long as there are
new requirements for producers from the food industry
around the world. Thus, for operators of food producers to
be certified as ISO, an HACCP a plan must be drawn. The
implementation of an HACCP system is a laborious work
specific to each company.
TABLE 7. The main actions related to maintaining the HACCP
system
Nr. crt. Action Term
1 Internal Audit Quarterly
2 HACCP plan reassessment Annual
3 HACCP plan review If the changes
4
Analysis of deviations from critical
limits at the PCC
Quarterly
5 Case review of complaint trends Monthly
6 Simulation procedure recall Annual
7 Technical News As appropriate
8
Analysis of training and retraining for
operating requirements
Quarterly
REFERENCES
1. Van Looveren L., Directiva 1993/43/EEC - Igiena alimentelor
HACCP-Codex Alimentarius, 2007.
2. ***, Ghidul national de bune practici pentru siguranţa alimentelor –
Sistemul de siguranţa alimentelor HACCP, Editura Uranus, Bucuresti,
2006.
3. Teodoru, T.. Implementarea şi certificarea sistemelor de management,
Editura Conteca 94, Bucuresti, 2004.
4. Heghedus-Mindru G., Biron R., Perju D., Rusnac L., Rivis A. and Stef
D., Journal of Food, Agriculture and Environmental , 6 (3- 4), 2008, 506,.
5. ***, Fisa tehnica interna a produsului – S.C. Fornetti S.R.L.
6. ***, Manualul de calitate – S.C. Fornetti S.R.L.
7. Ionete E., Buhanca M., Tusca A., Cristea A., Stoian D., Marin V. D.
and Buga C.R., Produse de patiserie si cofetarie. Ghid national de bune
practici pentru siguranta alimentelor, Ed. Uranus, 2006.
8. ***, STAS 91/83 - Produse de patiserie si cofetarie, 1983.
Received: 10 January 2011
Accepted: 20 May 2011

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HACCP plan for pastry

  • 1. Chemical Bulletin of “Politehnica” University of Timisoara, ROMANIA Series of Chemistry and Environmental Engineering Chem. Bull. "POLITEHNICA" Univ. (Timisoara) Volume 56(70), 1, 2011 47 Quality Control of Pastry Products using the HACCP Method M. Panfiloiu* , M.C. Cara** , D.M. Perju*** and G.A. Dumitrel*** * S.C. Antarctica S.R.L. Timisoara, Sanmihaiul Roman Nr.526A, Romania, mirabelapanfiloiu@yahoo.com ** Sanitary-Veterinary and Food Safety Directorate of Timis, Surorile Martir Caceu 4, Timisoara, Romania *** POLITEHNICA University of Timisoara, Industrial Chemistry and Environmental Engineering Faculty, 300006, 2 Victoriei Square, Timisoara Romania, Phone:+40-256-403073; Fax:+40-256-403060 Abstract: HACCP is a procedure that companies have to apply in order to protect the quality of food products. The purpose of this paper is to describe the critical points in which hazard can come to light in the production process, the evaluation and the measures applied to prevent and control these critical points. This method is applied to all the technological processes in order to obtain the pastry products without yeasts. Keywords: pastry products, hazard analysis, critical control points. 1. Introduction HACCP is an acronym for “Hazard Analysis and Critical Control Points”. It is a preventive method used for increasing the safety of food, cosmetics and drugs. The method appeared in 1971 in the U.S.A. The European Community has promoted since 1983 introduction of HACCP principles in its legislation. In the EU Council Directives on food hygiene HACCP is a concept as well as a method of operation, applied to all phases of food production. The purpose of these directives is to encourage food manufacturers and retailers in the application of HACCP in their own companies. In the UK, in September 1995 a mandatory application of HACCP has been instituted in all links of the food chain [1]. HACCP is a scientific system of self control of the manufacturing process, which has been extensively used in food production to prevent problems that may occur, using the critical control points (CCP) in manufacturing process, where the risk can be controlled, reduced or eliminated. A company must have a real system to meet requirements and prevent spoilage of products. It is a system that controls the relevant hazards to food safety, through Critical Control Points (CCP). A CCP is defined as a point, step, or procedure in a food manufacturing process at which: - control that is essential to prevent or eliminate a food safety hazard or reduce it to an acceptable level can be applied; and where, - later processing steps won’t correct these safety problems [2]. If one of the parameters of the CCP are out of control it is possible to reach the compromise of food safety. Unlike Critical Control Point, Control Point (CP) is any step in the process at which biological, chemical, or physical risks or hazards can be controlled, and usually is related to quality or production issues and not to product safety, unless the control point supports a CCP. The hazard is any physical, chemical, biological agent or body, which, if present in the food in the moment of consumption, has the capacity to affect the innocuity or the hygienic quality of the product. A critical limit is defined as 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 to an acceptable level, the occure of a food safety hazard. A critical limit is used to distinguish between safe and unsafe operating condition at a CCP. By monitoring CCP, the elimination of the risk is ensured or the risk is reduced by keeping it at levels below the critical limit. The monitoring of CCP means observation and planned measurement of risk from that critical control point. It is achieved through: inspection, sensory assessment, physical records, chemical analysis and microbiological analysis. Following an international statistics, it appeared that the ratio of chemical and biological hazards is 1/100 000. The laws of our country require that mandatory implementation of HACCP system, not its certification. Some benefits of implementation or certification of the system are: - A quality system that ensures food safety meaning that the food will not affect consumers if food is prepared or consumed as indicated; - Is the guarantee for the production and trade of safe food, being transparent, both for official inspection, and consumers; - Is a quality system "urged" by retailers (who are first in contact with customers and stakeholders to market safe products); - Is a system that minimizes risk over the technological process [3]. HACCP implementation is related to determining in advance the rules of good practice on the following: construction, machines location, technological process, personnel, cleaning and disinfection, pest control, raw and auxiliary materials used, including water, product traceability, transport. HACCP team should be multidisciplinary and include a motivated member of the executive management who is
  • 2. Chem. Bull. "POLITEHNICA" Univ. (Timisoara) Volume 56(70), 1, 2011 48 able to provide necessary financing and general motivation of the company to ensure successful implementation of HACCP. HACCP team will also need a well educated person who will lead the implementation of HACCP. The team should include multidisciplinary specialists: who understand biological, chemical and physical hazards associated with a particular group of products, who are responsable or involved in production / manufacturing of products, who have experience and practical knowledge of hygiene, and working process and function of the equipment operating within the organization, as well as other specialists with appropriate knowledge in microbiology, hygiene and food processing technology [5]. Optimally, a multidisciplinary team will be built within the organization. But which lacks the necessary experience, the team should be assisted by qualified specialists/ experts to help them resolve difficulties, including risk analysis, control and determination of the critical control points. Experts can be from the commercial and industrial associations, independent experts and regulatory authorities. HACCP plans are developed by the HACCP team and approved by the General Manager of the Company. Distribution of documents is based on the distribution list, so that at any moment the workplace where they were broadcast is known. Along with the distribution of documents available, obsolete documents are promptly removed from all points of distribution, by the concern of the elaboration unit. After withdrawal invalid documents are destroyed or identified by writing "invalid". Change documents may be determined by revising the organization and functioning of society, reference documents (regulations, rules, laws, etc.) and applications employees / customers / suppliers / external organizations. Because the information contained in the records must be complete and easy accessible, forms are used. That forms offer directions regarding the data that has to be recorded. By their format they provide indications of data to be recorded. Encoding of the forms is made by Quality Officer in accordance with regulations: “The development and codification of procedures, work instructions and HACCP plans”. The preservation of the documents is for a specified period of time. Verification of the HACCP plan will be made quarterly. Tests and other evaluation methods will be applied in order to determine if the system is effective [6]. Tests will be applied on: The production process - Analysis of process deviations that occur - Analysis of corrective measures taken 2. Conditions of production - hygiene plan testing - maintenance plan testing - testing the method of recording and handling complaints from customers - Testing the training method 3. Final products - a quality control of the product is made by sampling the final product. Plan review will be made annually or if changes occur in conditions or methods of operation: - Changing raw materials, ingredients or primary packaging - Acquiring new equipment or other changes in processing conditions - Changes in the technological flow - Changes in legislation - Changing equipment The present paper aims at identifying and monitoring potential risks in the process of cheese pastry, and implementation of corrective actions in order to restore critical control points within acceptable limits. 2. Experimental The product considered in this paper is a pastry product made from dough without yeast, with a homogeneous cheese-based filling. The product is distributed frozen, roasting and selling being achieved at the point of working partners [5]. Raw materials and materials used in the manufacturing process are presented in table 1. TABLE 1. Raw materials and materials used in the manufacturing process Name of raw materials Quantity % Meal 32.23 Water 27.84 Margarine for puffs 25 Cottage 15 Sour 3 Thickener 2.33 Milk replacer powder 1.15 Salt 0.87 Acidifying 0.58 Sugar 0.29 Dyes 1.36 In table 2 (Physicochemical characteristics) and 3 (Microbiological characteristics) are showed the physicochemical and microbiological characteristics of the studied frozen product [5]. TABLE 2. Physicochemical characteristics Features Conditions of eligibility Verification methods Content filler% 25-30 STAS 91/83 Fat content,% 30-35 STAS 91/83 Total salt,% 1-3 STAS 91/83 Humidity,% 40-45 STAS 91/83 TABLE 3. Microbiological characteristics Features Verification methods Limits Escherichia coli ISO 16649-2/2002 Absent Salmonella SR EN ISO 6579/03 Absent Stafilococus coagulazopositiv SR EN ISO 6888-1/2002 Absent Packaging of the finished product is in printed polyethylene bags and PVC boxes and the closure of the bags is made by thermal closure. The storage is made by freezing at least -18 ± 3°C, protected from external effects. The transport is made with special vehicles so that the cold chain is respected, and that no changes will occur [5].
  • 3. Chem. Bull. "POLITEHNICA" Univ. (Timisoara) Volume 56(70), 1, 2011 49 3. Results and Discussion Potential risks were identified in the process of cheese puff pastry. Then the risks have been evaluated using the criteria resulted from the severity and frequency of risk occurrence. Gravity is the consequences suffered by a consumer from exposure to a contaminant and is divided as follows: -High (3 points) - fatal consequences, serious illness, incurable damage that occurs either immediately or after a longer period - Media (2 points) - substantial damage and / or illnesses - Small (1 point) and minor injuries or illness, minor effects or no effects at all. Frequency is the probability to have a contaminant in the final product upon consumption. Probability is determined by measurements or observations during certain specific situations arising during the manufacturing process. They are classified as: - Small (1 point) - virtually impossible to produce or improbable - Media (2 points) - can occur, they happen to occur - High (3 points) – it occurs systematically. Stability risk class was made taking into account the four possible levels: level one - no measure of control (f × g = 1), level 2 - without control measures, but in risk analysis you take into account this risk (f × g = 2; 3), level 3 - general control measures for possible control points (f × g = 4), level 4 - specific control measures to eliminate or reduce risk to acceptable levels (f × g = 6;9). Control measures were established for each risk. HACCP team has determined the critical control points through the “Decision tree method”, analyzing risks of 2,3,4 degree [7]. Figure 1 “A decision tree” is presented to identify critical control points. Figure 1. Decisional tree The critical control points for pastry without yeast have been determined at all stages of the technological flow (figure 2). Figure 2. Technological flow chart Table 4 presents only those stages of the production process, which will be monitored to eliminate non- compliance. For each critical control point acceptable limits were set, taking into account the existing regulatory requirements and manufacturing technology. When critical limits of critical control points have been reached or are about to be reached, the product is identified and isolated and will be treated as non-compliant product. To restore the process within the default parameters of the manufacturing technology and in order to restore the critical control point within the allowed limits, corrective actions are established following the steps: 1. Analysis of identified problems is made in order to determine their causes, for taking correct decisions for corrective actions. The analysis of deficiencies occurred is made by the HACCP team. In its analysis, the main problem is breakdown in partial problems and a hierarchy of importance is established. Once the individual influences of each second problem on the main problem is established, the causes of the second problem are identified. 2. The establishment of the causes of the existing problems is made after the analysis performed by the HACCP team.
  • 4. Chem. Bull. "POLITEHNICA" Univ. (Timisoara) Volume 56(70), 1, 2011 50 Possible causes of identified or potential problems are: - Inadequate or nonexistent procedures and instructions - Failure of procedures or instructions - Lack of control of the processes - Lack of appropriate training - Improper working environment - Financial and human resources inadequate or insufficient. 3. The establishment and the implementation of corrective actions is made in order to remove causes of the existing non-compliances. HACCP team established methods for monitoring critical control points (CCP) and the correct actions required to be applied when exceeding the critical limits established. In Table 5 methods are presented through which are made: monitoring, frequency and corrections to be applied to eliminate risk. In order to restore critical control points within the allowed limits, responsible have been designated for monitoring the steps taken into discussion and other responsible which will deal with the implementation of corrective actions. Recordings will be made according to a pre-verification program. In Table 6 appointed responsible are presented, and also the records that have to be made regarding the applicability of corrective actions. TABLE 4. Critical control points “Decision tree” questions No. Stage of technological process Risk Risk class Q1 Q2 Q3 Q4 CCP 1. Screening / dosing flour F-foreign body 4 YES YES - - YES 2. Freezer M–microbiological development 3 YES NO YES NO YES 3. Packaging / weighing / metal detection F-foreign body 4 YES YES - - YES 4. Cold storage M– microbiological development 3 YES NO YES NO YES 5. Unloading cars at the premises and the partners M–microbiological development 3 YES NO YES NO YES TABLE 5. Monitoring, frequency and corrections Critical value MonitoringStage of technological process Risk Parameter Allowable limit Method Frequent Corrective actions Screening / dosing flour F foreign body Absent Cleaning and checking sites Weekly Replacement sites Freezer M Core temperature of frozen product Maximum - 13°C Thermometer measurement kernel -freezer shock:each trolley; -tunnel freezer: each kneading -Declaring non-compliant product - Prohibition of leaving the cold store frozen products 72 hours min Packaging / weighing / metal detection F Metal objects Feros ∅2,0 mm Neferos ∅2,0 mm steel ∅3,0 mm Metal detection, verification standards Each package of frozen, from 3 to 3:00 hour random download Declaring non-compliant product Cold storage at headquarters and in the premises of M Storage temperature + 18±3°C Monitoring parameters storage Standing on the viewing display, scoring 6 times per day -Technical department store closing -Announcement, application services provider of cold air service, - Declaring non-compliant product Unloading cars at the premises and the partners M Core temperature of frozen product Maximum - 13°C Thermometer measurement kernel Every download -Declaring non-compliant product; -Prohibition of leaving the cold store frozen products 72 hours min
  • 5. Chem. Bull. "POLITEHNICA" Univ. (Timisoara) Volume 56(70), 1, 2011 51 TABLE 6. Responsible for implementing corrective actions and for monitoring Stage of technological process Responsible monitoring Responsible for implementing corrective actions Recordings Screening / dosing flour Appointed Technical Department Head of technical department "Weekly checks Schedule" Freezer Packer -Department quality-control product -Commission analysis of non- compliance "Application of shock freezing" "Application of freezing tunnel" "Report of noncompliance" Packaging / weighing / metal detection - Metal-detector - Chief packing, respectively -Department quality-control product -Department quality-control product "Application of product verification parameters" "Report of non-compliance items" Cold storage at headquarters and in the premises of Chiefs and heads of exchange deposits -Chief Deposit - Technical Department - Department-product quality-control "Track temperatures in frozen food store" - headquarters "Table for the notation temperatures" work-points Store bosses at the premises - Commission of Analysis of non- compliance - Heads of deposits Receiving frozen-Register -Report of noncompliance Unloading cars at the premises and the partners Drive-in partners Transport logistics department Transport bosses "Centralized route" "Report of non-compliance items" 4. Conclusions HACCP examines the way of the development of food production, the distribution, the evaluation of the risk points, physically, chemically and microbiologically and elaborates the ways to prevent hazards and the ways to reduce risks. Food Safety System - HACCP works by rules of good hygiene and manufacturing practices, procedures and instructions, appropriate training, discipline and conscientious, good communication, accurate and complete registration system and monitoring the CCP[4]. System efficiency can be proven by a safe finished product on which microbiological and physicochemical analysis do not indicate dangerous contaminants outside the established maximum limits, no complaints, no major deviations in the CCP, increased product market request and little corrective action. Maintaining the system of frozen food safety operational, is assured by providing a plan of main actions of the scheme. The main actions related to maintaining the HACCP system are presented in table no 7. Communication is an important factor in the smooth implementation and operation of the HACCP system, as this ensures a continuous link between all departments involved in the action and also a good connection between the departments and the HACCP team. HACCP programs are necessary as long as there are new requirements for producers from the food industry around the world. Thus, for operators of food producers to be certified as ISO, an HACCP a plan must be drawn. The implementation of an HACCP system is a laborious work specific to each company. TABLE 7. The main actions related to maintaining the HACCP system Nr. crt. Action Term 1 Internal Audit Quarterly 2 HACCP plan reassessment Annual 3 HACCP plan review If the changes 4 Analysis of deviations from critical limits at the PCC Quarterly 5 Case review of complaint trends Monthly 6 Simulation procedure recall Annual 7 Technical News As appropriate 8 Analysis of training and retraining for operating requirements Quarterly REFERENCES 1. Van Looveren L., Directiva 1993/43/EEC - Igiena alimentelor HACCP-Codex Alimentarius, 2007. 2. ***, Ghidul national de bune practici pentru siguranţa alimentelor – Sistemul de siguranţa alimentelor HACCP, Editura Uranus, Bucuresti, 2006. 3. Teodoru, T.. Implementarea şi certificarea sistemelor de management, Editura Conteca 94, Bucuresti, 2004. 4. Heghedus-Mindru G., Biron R., Perju D., Rusnac L., Rivis A. and Stef D., Journal of Food, Agriculture and Environmental , 6 (3- 4), 2008, 506,. 5. ***, Fisa tehnica interna a produsului – S.C. Fornetti S.R.L. 6. ***, Manualul de calitate – S.C. Fornetti S.R.L. 7. Ionete E., Buhanca M., Tusca A., Cristea A., Stoian D., Marin V. D. and Buga C.R., Produse de patiserie si cofetarie. Ghid national de bune practici pentru siguranta alimentelor, Ed. Uranus, 2006. 8. ***, STAS 91/83 - Produse de patiserie si cofetarie, 1983. Received: 10 January 2011 Accepted: 20 May 2011