132/2008 Sb.
DECREE
from day 4. April 2008
on the quality system in the implementation and provision of activities related to the
the use of nuclear energy and radiation activities and assurance
the quality of the selected devices with regard to their inclusion in the
safety classes
State Office for nuclear safety shall be determined according to § 47 para. 7 to the
implement section 2 (a). I), section 4, paragraph 4. 8 and § 13 para. 3 (b). (d)) and paragraph 2. 5
Law No. 18/1997 Coll. on peaceful uses of nuclear energy and
ionizing radiation (the Atomic Act), and amending and supplementing certain
laws, as amended by Act No. 13/2002 Coll. and Act No. 253/2005 Coll.:
§ 1
The subject and scope of editing
This Decree regulates the
and quality) system requirements on the implementation or provisioning activities
associated with the use of nuclear energy or radiation activities
(b)) the requirements for filling a quality assurance programme
(c)), the criteria for inclusion and the distribution of the selected device to the
safety classes
(d)) the basic requirements for quality assurance of selected device
in view of their inclusion in the safety classes and
(e)), the scope and the implementation of the list of selected devices.
§ 2
Tiered access
Anyone who introduces a system of quality, apply a tiered approach.
A tiered approach must take into account the
and the complexity of the process, activity), their inputs and outputs and their significance
in terms of nuclear safety and radiation protection,
(b)) the classification of ionizing radiation sources, way of dealing with them and
the category of the site at which the radiation activities
(c)) the treatment of nuclear materials and radioactive waste management
provided for by other legislation "^ 1") and
(d) the inclusion of the selected devices to) security classes according to § 12.
§ 3
General requirements for the quality system
The quality system must be
and) designed processes and activities, related to the quality of the items, including
products, affecting nuclear safety or radiation protection (hereinafter
"the processes and activities"), their inputs and outputs, including their
the potential impact on nuclear safety or radiation protection,
b) sequence and interrelationship of processes and activities,
c) processes and activities are planned, managed, executed, authenticated and
evaluated so as to achieve the quality of the items with respect to its
importance in terms of nuclear safety, radiation protection, or
(d)) used by the acceptance criteria and methods for planning, management,
the implementation, validation and assessment of the processes and activities
(e)) established the organizational structure and its changes, including the rights,
obligations and the reciprocal relationships of persons processes and activities planned,
controls are carried out, verified or evaluated in order to ensure their effective
synergies,
(f)), there is a way to communicate within an organizational structure and method
communication with people different from the subject of the quality system,
that the implementation of processes and activities involved in, or to which processes
and activities are directed,
g) set out the requirements on suppliers who are involved in the implementation of the
processes and activities
h) performed monitoring and control of processes, activities, inputs and
the outputs in terms of their quality requirements to demonstrate compliance
their properties with the requirements prescribed in the system documentation
the quality,
I) modalities and criteria for the evaluation of the quality system of the continuous
with regard to its efficiency; evaluation of the quality system, shall be carried out
1. the persons responsible for the evaluation of its own activities pursuant to § 5 in them
control areas of the quality system and
2. the independent evaluation of the quality system cleared persons who
participate in the planning, management or execution of a process or activity,
which are the subject of reviews,
j) secured the personnel, technical, material and financial resources,
including a suitable working environment, needed to maintain and improve the
quality system and for the implementation of the processes and activities and to deploy,
maintain and continuously improve their effectiveness,
k) applied measures to improve the quality of items affecting
nuclear safety or radiation protection,
l) carried out improvement of the quality system by the application of corrective and
preventive measures based on the results of the evaluation.
§ 4
The requirements for the documentation of the quality system
(1) any person who establishes a system of quality, it must be documented.
The quality system documentation includes
and a document describing the quality system) with regard to General requirements
pursuant to § 3,
b) documented procedures describing processes and activities within the system
quality and their management and implementation,
c) working documents following the documented procedure in detail
describing the way of planning, verification, implementation, reviews and proceedings
process or activity and the evaluation of the quality system, including their
outputs or product specifications; the working documents are, in particular,
manuals, instructions, rules, rules, training plans,
programs, documents or drawings for production in any medium, and
d) records demonstrating the activities performed or results achieved in
the performance of the quality system requirements or requirements for individual items
affecting nuclear safety and radiation protection, as set out in
documented procedures or in the working documents.
(2) the quality system documentation must be
and easy to understand, complete) uniquely identifiable, traceable and to
available as amended to all persons carrying out relevant activities,
(b)) prior to the introduction in terms of reviewing the suitability,
adequacy, effectiveness, clarity, correctness, and completeness, and
approved persons designated and
c) safely stored and archived for a period fixed by other legal
Regulation ^ 2) or, if the time is not for a specific document archiving as follows
established, for a period specified by the documented procedure for process
Archiving; time to archive records concerning quality assurance
the selected device is laid down in § 13 para. 2.
§ 5
Persons in the system of quality
(1) within the quality system shall be determined by the persons responsible for the
and the maintenance of the quality system) in accordance with the General requirements under section
3,
(b) documenting the process under §) 4 (4). 1 (b). b) to (d)),
(c)) to ensure effective interaction and links between processes,
(d) ensuring and documenting compliance) the output of the process with the requirements of the
This output laid down in the quality system documentation,
e) recording and monitoring during the process,
f) resolve disagreements processes and their outputs,
g) evaluating the effectiveness of the process and its changes and
h) support for process improvement.
(2) a person designated within the quality system referred to in paragraph 1 shall be
established rights and obligations necessary to carry out the intended entrusted to them,
activities.
§ 6
Processes and activities
(1) planning, management, verification, implementation and evaluation processes, and
activities in the quality system must be carried out by persons with qualifications
appropriate to the type and importance of their work. This qualification
the lowest allowable is achieved by determining the qualifying
requirements on such persons by ensuring that their training and assessment
the effectiveness of the training so that these persons can carry out allocated
activity and have notice the influence of its activities on nuclear safety
or radiation protection. The qualification of such persons, including their
education and training must be documented.
(2) processes and activities must be planned and carried out under the following
terms and conditions:
and) documented procedures and working documents relating to the item
affecting nuclear safety or radiation protection are available,
(b)) the implementation of processes and activities are in conformity with the requirements of the documented
the procedures and the working documents for processes and activities,
(c)) is used in the proper equipment for the implementation of the processes and activities and are
secured the necessary working conditions and environment for their implementation,
(d)) performs monitoring and checking the properties of items affecting
nuclear safety or radiation protection,
(e)) production, monitoring, measuring or test equipment is maintained in
enabling the State to demonstrate the achievement of permanent line items affecting
nuclear safety or radiation protection with skill requirements;
for the control, monitoring, calibration and maintenance of measuring and testing
the device will process the procedures to ensure that the measurement uncertainty
corresponds to the required competency measurement, and
f) changes to the processes and activities shall be carried out only on the basis of the proposal,
substantiated and zhodnoceného in terms of the purpose of the change and its impact on
nuclear safety or radiation protection, and demonstrate the impact of the changes on the
level of nuclear safety and radiation protection afterwards.
(3) every process within the quality system must be evaluated in terms of
efficiency. Evaluation of the effectiveness of the process must be carried out by comparing the
the outputs of the process with the requirements imposed on it in the system documentation
the quality.
(4) the processes and activities should be subjected to review to confirm
the suitability, adequacy and effectiveness of the items affecting the nuclear
safety or radiation protection (hereinafter referred to as "the review"), authentication to
confirm the line items affecting nuclear safety or radiation
with the requirements of the protection of its property (hereinafter referred to as "verification") and validation
to confirm the line items affecting nuclear safety or
radiation protection, with the requirements of its intended use (hereinafter referred to as
"validation"). For the review, verification and validation of processes and activities
must be determined and documented the schedule, scope, method of implementation
the review, verification and validation and acceptance criteria and must be
determined by the responsibility of persons for compliance with these criteria. The examination,
verification or validation processes can perform only the person responsible for
activities referred to in section 5, and at the same time a person different from those people that are
-participating in the implementation of the process or activity. The results of the examination,
verification and validation of processes and activities are documented in the form of
records.
(5) If, in the course of a process or activity in the documented
procedures or working documents established checkpoints, you cannot
process or activity to continue without demonstrable consent
the designated person, issued on the basis of status or result of the validation check.
(6) the requirements for the processes carried out by the supplier shall be given in the documentation
the quality system pursuant to § 4 paragraph 2. 1.
§ 7
Some processes requirements related to the product
(1) the process of designing the product, including development, design, and
designing the product, (hereinafter referred to as the "design process") must be further considered
the following conditions:
and review of inputs) is performed in the design process from the viewpoint of nuclear
safety and radiation protection to evaluate their compliance with the requirements of
other legislation relating to the product and with the agreed
specifications,
(b)) is performed a review of the design process to evaluate the ability of
the output of the design process to meet the requirements set out in the inputs and
the requirements, which are a prerequisite for the intended use of the product,
(c)) is performed in the design process validation to determine if the outputs of the
the design process comply with the applicable legal requirements and
laid down by the specification relating to the product with regard to nuclear
safety and radiation protection, and whether it is determined how to resolve imbalances
from these requirements,
(d) the final output) will process the documentation of the design process, including
putting its changes in a form that will allow its verification in relation to
inputs for the design process by qualified persons, which participated in the
its processing, or by independent qualified persons and
e) validation of the design process is carried out to determine whether the proposed
the product according to the final output of the design process documentation meets the
the requirements for the intended use in terms of nuclear safety or
radiation protection.
(2) the process of production of the product must be carried out on the following conditions:
and product specifications), including its amendments, is in accordance with the technical
regulations, technical specifications or technical standards, which
include the applicable requirements of other legislation for
nuclear safety and radiation protection,
(b) the method of manufacture of the product) is documented in accordance with the requirements of
set out in the final output documentation for the design of the product,
(c)) is determined by the type, method and scope of the review, verification and validation
the product, including acceptance criteria, before its intended use,
(d)) the product is unmistakable way identified and this identification
to maintain,
(e)) are available for information about current or past status, location, and
use of the product, or on the current or past treatment
product at any time during the production process,
(f)) the product is supplied in a State that allows authentication and
g) match product with the requirements specified in the documented
the procedures and the working documents for its production is documented
records.
(3) the process of procuring the product must take place on the following conditions:
and the documentation for the procurement) are set correctly and completely
the requirements for the product, including the requirements of quality assurance
of the product. The documentation for the procurement and the requirements shall be specified on the
reporting and address the identified mismatches,
(b)) in the course of the procurement process is carried out supervision of contractors,
(c)) are established in advance in the requirements for the selection and evaluation of suppliers
product based on their ability to supply product; product vendors
are selected and evaluated on the basis of those requirements, and
(d) conformity of the delivered products with) the prescribed requirements for procurement is
documented records that are available before using the product.
(4) the processes and activities in the transport, storage and maintenance of the product
must be carried out in a manner which prevents damage, unintended use
or destruction of the product.
(5) the requirements for processes whose compliance with these requirements cannot be in
full validate subsequent inspection or test of the product, in particular
on the forming, welding, non-destructive testing, heat treatment,
creation of software or computing resources,
the implementation of medical exposure of patients (hereinafter referred to as "special processes")
must be laid down in the product specification, which is a special
processes apply. Special processes be governed, validate, implement and evaluate
only sufficiently qualified persons whose knowledge and skills must
be regularly audited and demonstrably. To the implementation of the specific
processes may be used only for technical equipment is regularly
compliance with the requirements of the project, the specific processes. The fulfilment of the
qualification requirements and verify compliance with the requirements of the Special
processes must be kept.
§ 8
Management of the divisions and their correction and preventive measures against conflicts
(1) the processes and activities, their inputs and outputs, which are not in conformity
with the requirements laid down in the schedule referred to in section 4 (hereinafter referred to as "mismatch
the entry "), are subject to the process of management disagreements.
(2) the process of management disagreements in the quality system, shall be carried out in accordance with the
the requirements of section 6 (1). 2 and in accordance with a documented procedure for the management of
disagreements that must provide for
and requirements for the implementation of identification) disagreement immediately after its
finding and documenting,
(b)) the requirements for the notification process to the relevant responsible persons of mismatches
the subject of the quality system,
(c)) treatment do not agree the entry and the requirements in order to avoid
the inappropriate use of non-conforming items, including the removal of disagreements, and
d) requirements for evaluation of the consequences and possible other effects of mismatch
for nuclear safety or radiation protection when using mismatched
item.
(3) to remedy the non-conformity must be in accordance with a documented procedure for
the management of disagreements to ensure
and the review of the non-conforming items)
(b) an analysis of the causes of disagreement)
c) determine how the solution of disagreement,
(d) evaluation of the necessary measures) to prevent recurrence
the occurrence of mismatches and
e) determination, documentation and implementation of appropriate remedial measures
the consequences of disagreement.
(4) to avoid disagreements that might arise (hereinafter referred to as "potential
mismatch "), must be processed and introduced documented procedure for
the exclusion of potential discord, which lays down requirements for the
and finding potential disagreements and) their possible causes,
(b) assessment of the necessary measures to) prevent the occurrence of potential
disagreements and
c) determining, documenting and the introduction of preventive measures of reasonable
the potential impact of potential disagreement; to determine the preventive
It uses its own measures of operational experience and operational
the experience of other bodies, if they are available.
(5) corrective or preventive measures Imposed must be kept
monitored and evaluated in terms of the status of their implementation and
efficiency.
§ 9
The quality system at the implementation or securing radiological activities
(1) the quality system at the implementation or securing radiological activities
in the workplace (IV). category must comply with the requirements of § 3 to 8.
(2) in the implementation of the quality system or the provision of radiological activities
in the workplace III. category must comply with the requirements of section 3 (b). a) to
(h)), (b). (I) point 1 (a)). j) to (l)), § 4, 5, § 6 (1). 1 to 5, § 7
paragraph. 3 (b). a), (c)) and (d)), para. 4 and 5, § 8 para. 1 to 3 and odst. 5.
(3) the quality system at the implementation or securing radiological activities
at work II. category and in the implementation of personal dosimetry and
other services relevant from the point of view of radiation protection shall comply with the
the requirements of section 3 (b). a) to (h)), (b). (I) point 1 (a)). j) to (l)), § 4, 5,
§ 6 para. 1-3, para. 5, § 7 (2). 3 (b). and) and (d)), para. 4 and 5, § 8
paragraph. 1 to 3 and odst. 5.
(4) the quality system at the implementation or securing radiological activities
in the workplace category and in the training of selected
workers must meet the requirements of section 3 (b). a) to (h)), (b). (j)), and k), section
4, 5 and § 8 para. 1.
§ 10
The requirements for filling a quality assurance programme for povolované
activities pursuant to § 9 para. 1 (b). a) to (g)), (b). I), (j)), n) and r)
the Atomic Act
(1) the Program shall document the quality assurance system in place
the quality. The filling of the quality assurance programme for povolované activities
According to § 9 para. 1 (b). a) to (g)), (b). I), (j)), n) and r) of the Atomic
the law must comply with the requirements of section 4, paragraph 4. 2 and be subject to regular
revisions that it brought in line with any changes made to the
the quality system.
(2) quality assurance programme must include
and the subject's identifier information), whose quality system program
quality assurance documents (the "submitter"); u
legal person, company or business name, registered office and identification form
number, if assigned; for natural persons first and last name, date of
of birth and address of the place of residence or other residence on the territory
The United States, or the address of the place of residence outside the territory of the Czech Republic,
(b)) the subject, location, and scope of activities of the petitioner,
(c)), with the exception of the workplace III. and the lower categories of personally identifiable information
direct suppliers of products used by the submitter; for legal
person, business name or the name, registered office and identification number, form,
If it was allocated; for natural persons first and last name, date of birth and
address of the place of residence or other residence in the territory of the United
Republic or the address of the place of residence outside the territory of the Czech Republic,
d) enumerate processes and their belonging to the activities for which the programme
quality assurance covers, showing the processes and activities
carried out by the supplier in a manner
e) documented procedures or references to these procedures with their
a unique identification,
(f) a description of the quality system) promoters including
1. responsibilities, rights and obligations and the reciprocal relationships of persons
plan, manage, validate, implement, evaluate processes and activities,
2. mutual relations and breakdown of the departments or work groups involved in
in the planning, management, verification, implementation and evaluation processes, and
activities, including the method of control and communication within the body with its
the vendor,
3. the principles of the quality system requirements and quality assurance
the quality of the processes, activities and products related to povolované
activities, including links to documented procedures
g) with the exception of the workplace III. and the lower category, the scope and
the application of the requirements of this Decree on the quality system and to secure
the quality of the suppliers, including the method of evaluation of the quality system and
authentication of quality assurance for these vendors,
(h) the method and specify the frequency) of the independent reviews cleared system
quality, if it is carried out, including the manner and form of the results of
These audits, and
I) method and specify the frequency of revisions assurance programme
the quality.
§ 11
The requirements for filling a quality assurance programme for povolovanou
activity according to § 9 para. 1 (b). l) of the Atomic Act
The filling of the quality assurance programme for povolovanou activities under section 9
paragraph. 1 (b). l) Atomic law provides § 4 paragraph 2. 2 Decree No.
145/1997 Coll. on the registration and control of nuclear materials and their
a closer definition, as amended.
§ 12
The criteria for classification and distribution of the selected device in the security
classes
The selected device are classified and divided into safety classes 1, 2 and
3. In the annex, there are criteria for inclusion and distribution of selected
the device in the security classes.
section 13 of the
The basic requirements for quality assurance of selected device
in view of their inclusion in the safety classes
(1) the quality assurance of the selected device must be used
the quality system documentation processed in accordance with section 4, which is
refers to the processes and activities in the design, construction, putting into
operation, operation or decommissioning of the selected device, in particular
records relating to the selected device
and) concerning special processes pursuant to § 7 para. 5,
(b) the listed in the security class) 1 or 2, demonstrating compliance with
the quality requirements of the selected device and final output validation
documentation of the design process of the selected device from the viewpoint of compliance with all the
acceptance criteria imposed on the selected device, its parts, and to
the materials used for its manufacture, or
(c) the listed in the security class) 1 or 2-resistant pressure
the working fluid, documenting the defects that have been detected by checking and
removed how to perform repairs of selected devices and consciously
left defects which are further monitored.
(2) the quality assurance of the selected device must be carried out
records demonstrating compliance with the requirements on the quality of the selected device in the
scale and in a manner that will allow at any time to assess the status of the selected
device. These records, and the records referred to in paragraph 1 must be securely
stored and archived for the lifetime of the selected device,
starting with the design of the selected device and its parts, after his
decommissioning.
(3) in the design process of the selected device must be in the final output
documentation of the design process for the selected device included in the safety
class 1 or 2 intended
and tracking the lifetime) the criteria for the selected device, conditions for
treatment with your device and its operation and
b) acceptance criteria needed for the performance of its security features.
(4) when the procurement process for the selected device must be in advance
the agreed scope of the reviewed documentation system of quality vendor
the selected device in terms of compliance with the requirements on the quality of items
affecting nuclear safety or radiation protection referred to in
evaluating the factors listed in section 4, paragraph 4. 2 (a). b). Of this
a review of the record must be made.
(5) in the process of commissioning and the operation of the selected device must
be
and documented way to provide identification) to the selected device, and
obtaining and maintaining information about current or past status, location, and
the use of the selected device or the present or the past how
treatment with your device at any time during the process of putting into
service and operation,
b) handled, loaded and maintained plans and programmes carrying out checks
selected devices and plans and programmes, the implementation of the maintenance, repair and
reconstruction of the selected device and
(c)) use spare parts of the selected devices that meet the
the requirements set out in the specification of the selected device.
§ 14
The scope and method of making the list of selected devices
(1) the selected device shall be clearly identified prior to their obtaining
for a nuclear device and for each nuclear facility must be
documented in the form of a list of the selected device.
(2) the list of the selected device in the text section must identify the
each of the selected device, with an indication of their safety classes, and
the selected device has to be broken down in terms of the performance of their security
features. In the drafting of the list of selected devices must be
a) schematically shown technology systems and building parts that
contain the selected device, with an indication of their distinguished
safety classes and highlight the boundaries between the selected and the other
device or other parts of buildings, and
b) identification details of the selected devices marked and for more information
which is clearly obvious functions for the selected device in the system or
the location of the selected device in the context of the construction of a nuclear device.
(3) included in the list of selected devices must be rules for the
and determine the boundaries between systems), devices or parts of the construction of the nuclear
device means a security feature and other systems
the device or parts of the construction of a nuclear installation and
(b) the boundary between the) determination of the safety of selected classes
device.
(4) the list of selected devices in stage designing of nuclear equipment
must conform to the approved project documentation and in the phase of operation
the nuclear device to the actual implementation of a nuclear device.
(5) before making changes to the design of a nuclear installation on
the selected device to determine whether the consequences of its implementation does not affect the
nuclear and technical security negatively and whether there are changes in the
the list of selected devices.
§ 15
Transitional provisions
(1) the quality assurance system and quality assurance programs must be reported to the
accordance with the requirements of this order not later than two years after the acquisition of its
efficiency.
(2) quality assurance of selected equipment must be put into
accordance with the requirements laid down by this Decree within two years
After the entry into force of this Decree.
section 16 of the
Regulation (EEC)
Repeals the Decree 214/1997 Coll. on quality assurance in
activities related to the use of nuclear energy and the activities of the
leading to exposure and about the establishment of criteria for the classification and Division
the selected device in the security classes.
§ 17
The effectiveness of the
This Decree shall enter into force on 1 January 2000. May 22, 2008.
Chair:
Ing. Drábová, Ph.d. in r.
Annex
The criteria for classification and distribution of the selected device in the security
classes
1. Criteria for classification and distribution of the selected device to the
safety classes for nuclear facilities, which includes the
PWR
1.1. Selected devices included in the safety class 1 are
bordering the pressure device the refrigeration cycle of a nuclear reactor,
with the exception of those devices for which it is possible to compensate for the damage
normal system for refilling of refrigerant.
1.2. Selected devices included in the safety class 2
cover the nuclear fuel facilities bordering the pressure circuit
nuclear reactor coolant which does not belong to safety class 1 and
filling device safety function of the system of which they are a part of, and it
device
1.2.1. to shut down the nuclear reactor as necessary so that the
due to the expected operational event there has been fullest
the project, and to shut down the nuclear reactor to mitigate
the consequences of the maximum project accidents
1.2.2. in order to maintain a sufficient amount of coolant for the cooling of the active
the zone of a nuclear reactor during emergency conditions, where
no infringement of the pressure of the coolant circuit of a nuclear reactor, and, after
the aftermath of these conditions,
1.2.3. to ensure heat dissipation from the active zone of a nuclear reactor in
violation of boundaries of the pressure of the refrigerant circuit, so as to limit the
damage to the nuclear fuel,
1.2.4. for removal of residual heat from the active zone of a nuclear reactor in
during all operating conditions and for emergency conditions, where
There has been no violation of the integrity of the boundary of the pressure of the refrigerant circuit,
1.2.5. necessary to limit releases of radioactive substances from the hermetic
envelope during and in the aftermath of emergency conditions,
1.2.6. necessary for energy supply or for traffic control devices
included in the safety class 2 in carrying out their security
features.
1.3. Selected devices included in the security class 3 are
filling device safety function of the system of which they are a part of, and it
device
1.3.1. to prevent unacceptable transition processes in the reactivity,
1.3.2. for maintaining the nuclear reactor in the conditions of safe
unset, after all the activities, which led to its withdrawal, after each
from his unset,
1.3.3. to maintain a sufficient amount of coolant for the cooling of the active
the zone of a nuclear reactor in all States of normal and abnormal
operation of a nuclear installation in the project under consideration,
1.3.4. for heat dissipation of the safety systems until the end of the degree
heat dissipation,
1.3.5. for maintaining the exposure of the population and of workers of nuclear facilities
below specified limit values during and in the aftermath project
accidents and serious accidents, resulting in leakage occurs
radioactive substances and ionizing radiation from sources
outside the protective envelope,
1.3.6. for maintaining the environmental conditions inside a nuclear installation,
necessary for the operation of the safety systems and the access of workers to
performance of activities important to safety,
1.3.7. to prevent leaks of radioactive substances from irradiated nuclear
fuel transported or stored inside nuclear facilities outside
nuclear reactor cooling system during all conditions of normal and
abnormal operation,
1.3.8. rozpadového heat dissipation from the irradiated fuel storage
inside the nuclear facility outside the nuclear reactor cooling system,
1.3.9. to maintain sufficient fuel stored inside the podkritičnosti
nuclear facilities outside the nuclear reactor cooling system,
1.3.10. necessary for the discharge of radioactive substances under the restriction provided for
the limit values over all States of normal and abnormal operation
1.3.11. for energy supply or for traffic control equipment
to safety class 3 in the performance of their security functions,
1.3.12. to ensure the functional ability of the other device listed
in safety classes 1, 2 or 3 in the performance of their security
functions, with the exception of proceedings or of energy supply,
1.3.13. designed to prevent or limit the consequences of failures of other
devices, systems, or parts of the construction of a nuclear device, included in the
safety class 1, 2 or 3, whose failure could lead to
distortion performance of their security functions,
1.3.14. the secondary circulation, for which the calculation of the working media pressure when
the calculated temperature of more than 100th. (C) is greater than 4 MPa and lightness of the pipeline
is greater than DN 200, if they are not included in the safety class 2
While the border between the selected device and the other devices is the place
anchor the last swing limiter or similar device from the
the secondary circuit.
2. the criteria for the classification and distribution of the selected device to the
safety classes for nuclear installations for the storage of radioactive
waste
2.1. The selected devices included in the safety class 2
packaging files for storage of radioactive waste from the revised
nuclear fuel.
2.2. Selected devices included in the security class 3 are
device forming engineering artificial barriers and the facilities necessary for the
prevent leakages of radioactive substances and ionizing radiation into the
and the work environment over the limit values laid down in the course of all
the project States of operation.
3. The criteria for the classification and distribution of the selected device to the
safety classes for facilities for the storage of spent nuclear
nuclear fuel
3.1. Selected devices included in the safety class 2
3.1.1. packing files for the storage of spent nuclear fuel
3.1.2. equipment necessary to maintain the required podkritičnosti
nuclear material.
3.2. Selected devices included in the security class 3 are
device forming engineering artificial barriers and the facilities necessary for the
prevent leakages of radioactive substances into the environment and the working environment
over the limit values laid down in the course of all project traffic conditions,
including devices that monitor the packaging parameters for file
storage of spent nuclear fuel, essential for compliance with the limits
and conditions of safe operation of these devices.
4. Criteria for classification and distribution of the selected device to the
safety classes for nuclear installations for the storage of radioactive
waste and spent nuclear fuel and nuclear facilities for the production,
processing, storage, and storage of nuclear materials
4.1. Selected devices included in the safety class 2
4.1.1. packaging files for storing spent nuclear fuel and
radioactive waste resulting from the revised nuclear fuel,
4.1.2. equipment necessary to maintain sufficient podkritičnosti
nuclear material.
4.2. Selected devices included in the security class 3 are
device forming an additional barrier to prevent artificial engineering leakage
radioactive substances into the environment over a specified limit
values.
1) Decree No. 307/2002 Coll., on radiation protection, as amended by Decree No.
499/2005 Coll., Decree 145/1997 Coll. on the registration and control of nuclear
materials and their closer, as amended by Decree No. 316/2002
SB.
2) Decree No. 307/2002 Coll., as amended by Decree No. 499/2005 Coll.
