Introduction

In accordance with the TS EN ISO / IEC 17025 standard internal audit article, laboratories are required to operate an internal audit mechanism that meets the requirements of the standard. This training will provide a suitable environment in terms of interpreting the relevant articles of the standard in accordance with its purpose and evaluating the issue with different perspectives and examples for an effective internal audit.

Purpose of the training

To provide information on how an internal audit that meets the expectations of the TS EN ISO / IEC 17025 standard will be and to raise awareness about the contribution of the internal audit to quality management.

Who can participate?

Anyone who takes part in TS EN ISO / IEC 17025 quality management and laboratory applications can participate.

Prerequisite

Having sufficient knowledge and experience about TS EN ISO / IEC 17025 is very important for the effectiveness of the training. Those who do not have sufficient knowledge and experience about the standard are not recommended to participate.

The maximum number of participants is 20 people. Limiting the number of participants in this type of training is important for the efficiency of the training.

 Introduction

TS EN ISO 15189 Medical Laboratories - Requirements for Quality and Competence Standard, which is the basic document used by the Turkish Accreditation Agency (TÜRKAK) for the accreditation of medical laboratories, is an international standard that includes general requirements for the competence of medical laboratories.
The articles of the TS EN ISO 15189 standard reveal the general conditions of a laboratory’s quality management system and technical competence. The purpose of this 3-day training is to provide the participants with an accurate perspective on the interpretation of the standard.

Purpose of the training

In medical laboratories that can perform biological, microbiological, immunological, chemical, immunohematological, hematological, biophysical, cytological, pathological, genetic or other analyzes of materials taken from the human body and operated by state and foundation universities, public institutions / organizations, private law legal entities and real persons; It is aimed to establish a Quality Management System in accordance with the standard of "TS EN ISO 15189 Medical laboratories - Requirements for Quality and Competence", to convey the standard information required to verify compliance with the requirements of the standard and to consolidate this information with applications.

Who can participate?

Medical laboratories;

• Managers,
• Persons Responsible for Quality Management,
• Technicians, Related Employees,
• Those who want to learn about TS EN ISO 15189 Medical Laboratories Standard and want to improve themselves can participate in this training.

Prerequisite

There are no preconditions.  Participants are recommended to obtain TS EN ISO 15189 standard and bring their personal computers for training applications.

Training duration: 3 Days

The maximum number of participants is 20 people. Limiting the number of participants in this type of training is important for the efficiency of the training.

 Introduction

Good Laboratory Practice (GLP) is a quality assurance system that includes planning, conducting, monitoring, recording, archiving and reporting of health and environmental safety studies other than clinical studies, and management procedures.

The Turkish Accreditation Agency (TÜRKAK), as stated in the Law on the Establishment and Duties of the Turkish Accreditation Agency No. 4457 and the Regulation on Good Laboratory Practices Principles, Harmonization of Test Units, Good Laboratory Practices and Inspection of Studies, published in the Official Gazette No. 27516 dated March 9, 2010, the National Monitoring Authority has legal responsibility.

Test facilities wishing to be included in the Good Laboratory Practices Conformity Monitoring Program are inspected by TÜRKAK in accordance with the OECD Good Laboratory Practices Principles and an GLP  Declaration of Conformity is issued.

Purpose of the training

It is aimed to provide the participants with basic information about OECD Good Laboratory Practices Principles, OECD GLP Series Documents and Related Regulations.

Who can participate?

State and foundation universities, public institutions / organizations, private law legal entities and test units operating / planning to operate in the field of GLP;

·       Managers,

·       Persons Responsible for Quality Management,

·       Technicians,

·       Related Employees

Those who want to learn about OECD Good Laboratory Practices and improve themselves can participate in this training.

Prerequisite

There are no preconditions.  Participants are recommended to bring their personal computers for OECD Guidelines documents and applications on GLP.

Training duration: 2 Days

The maximum number of participants is 20 people. Limiting the number of participants in this type of training is important for the efficiency of the training.

 Introduction

Traceability of Measurements and Measurement Uncertainty Training is a training for measuring uncertainty components, determination, use and reporting in order to calculate the measurement uncertainty needed to determine the confidence level of the methods included in the service of the accredited or candidate (willing to be accredited) test laboratories. In addition, the training includes basic theoretical and practical knowledge on traceability of measurements to national and international measurement standards.

Purpose of the training

·       to inform the accredited test laboratories or those applying for accreditation, on the determination, use and reporting of measurement uncertainty in the methods within the scope of accreditation,

·       To inform the participants at a basic level about the traceability of measurements to national and international measurement standards,

·       Providing information on national and international policies and procedures regarding the Traceability of Measurements and Measurement Uncertainty,

·       It is aimed to include theoretical and practical applications in metrological traceability, SI Units and calculation of measurement uncertainty for testing laboratories.

Who can participate?

Anyone who is or will take part in the determination, use and reporting of measurement uncertainty in test / measurement results and anyone who knows a computer (Excel program) who wants to improve and improve themselves can participate in the training.

Measurement uncertainty training is a general training and does not include information on measurement uncertainty in specific test areas.

Prerequisite

·       Having received TS EN ISO / IEC 17025 - General Conditions for the Qualification of Testing and Calibration Laboratories standard training or having basic knowledge.

·       Having received Validation Training

·       Basic knowledge of mathematics and statistics may be useful for measurement uncertainty training.

·       Participants are required to bring their personal computers

The maximum number of participants is 20 people. Limiting the number of participants in this type of training is important for the efficiency of the training.

 

 

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 Introduction

TS EN ISO / IEC 17025 Standard, which is the basic document used by the Turkish Accreditation Agency (TÜRKAK) for the accreditation of test and calibration laboratories, is an international standard that includes general requirements for the competence of test and calibration laboratories. The articles of the TS EN ISO / IEC 17025 standard reveal the general conditions of a laboratory’s quality management system and technical competence. The purpose of this 3-day training is to give the participants an accurate perspective on the interpretation of the standard.

Purpose of the training

·       to give participants an accurate perspective on TS EN ISO / IEC 17025 Standard,

·       To contribute to the work of laboratories by interpreting the management and technical conditions clauses that form the basis of the standard,

·       It is aimed to provide the participants with basic information about TURKAK’s role in accreditation of test and calibration laboratories and accreditation processes.

Who can participate?

·       Laboratory managers,

·       Quality managers,

·       Calibration and test laboratory employees,

·       Anyone who wants to improve himself / herself regarding the General Conditions Standard for the Competence of Testing and Calibration Laboratories of TS EN ISO / IEC 17025 can participate in this training.

Prerequisite

There is no precondition to participate in this training. Participants are recommended to have the TS EN ISO / IEC 17025 Standard.

The maximum number of participants is 20 people. Limiting the number of participants in this type of training is important for the efficiency of the training.

 Introduction

TS EN ISO / IEC 17043 Standard, which is the basic document used by the Turkish Accreditation Agency (TÜRKAK) for the accreditation of proficiency testing regulators, is an international standard that includes general requirements for proficiency test and interlaboratory comparison test regulators. The articles of the TS EN ISO / IEC 17043 standard set out the general requirements for the quality management system and technical competence of the proficiency test regulators. The purpose of this 3-day training is to give the participants an accurate perspective on the interpretation of the standard.

Purpose of the training

·       To give the participants an accurate perspective on the TS EN ISO / IEC 17043 Standard,

·       To contribute to the work of laboratories by interpreting the management and technical conditions clauses that form the basis of the standard,

·       It is aimed to provide the participants with basic information about the role of TURKAK regarding the accreditation of Proficiency Testing Providers and the accreditation processes.

Who can participate?

·       Laboratory managers,

·       Quality managers,

·       Calibration and test laboratory employees,

·       Anyone who wants to improve themselves on the General Conditions Standard for the TS EN ISO / IEC 17043 Proficiency Test can participate in this training.

Prerequisite

There is no precondition to participate in this training. Participants are recommended to have the TS EN ISO / IEC 17043 Standard.

Training duration: 3 Days

The maximum number of participants is 20 people. Limiting the number of participants in this type of training is important for the efficiency of the training.

 Introduction

 For the reliability of the test results, it is important to select the appropriate method and to show that the chosen method meets certain conditions. According to ISO/IEC 17025, Before applying the chosen method to experiments, it should confirm that it can apply standard methods, as well as validate non-standard methods, methods designed / developed in the laboratory, standard methods used outside their intended scope, and standard methods supplemented or modified with additions to confirm that they are suitable for the intended use. Validation; It is the verification of the fulfillment of the necessary conditions for a special purpose use as a result of the examination and obtaining an objective evidence.

For this purpose, method performance parameters need to be determined and controlled. With this training, it is aimed to convey the knowledge in the field of validation to the participants by the experts of the subject.

Purpose of the training

It is aimed that the participants have information on the following subjects,

·       Purpose and Importance of Method Validation

·       Method Performance Parameters (Selectivity, LOD / LOQ, Accuracy, Precision etc.)

·       Calculation of Validation Data and Evaluation of Appropriateness (Using F test, t-test, ANOVA etc.)

Who can participate?

·       People who want to develop and improve themselves who will be involved in method validation and validation studies can participate in this training.

·       Validation training is a general training and does not include information on specific test areas.

Prerequisite

·       Having received TS EN ISO / IEC 17025 - General Conditions for the Qualification of Testing and Calibration Laboratories standard training or having basic knowledge

·       It is considered that it would be beneficial for the participants to have basic knowledge of mathematics and statistics.

·       Participants are required to bring their personal computers.

The maximum number of participants is 20 people. Limiting the number of participants in this type of training is important for the efficiency of the training.

 Introduction

 For the reliability of the test results, it is important to select the appropriate method and to show that the chosen method meets certain conditions. According to ISO/IEC 17025, Before applying the chosen method to experiments, it should confirm that it can apply standard methods, as well as validate non-standard methods, methods designed / developed in the laboratory, standard methods used outside their intended scope, and standard methods supplemented or modified with additions to confirm that they are suitable for the intended use. Validation; It is the verification of the fulfillment of the necessary conditions for a special purpose use as a result of the examination and obtaining an objective evidence.

For this purpose, method performance parameters need to be determined and controlled. With this training, it is aimed to convey the knowledge in the field of validation to the participants by the experts of the subject.

Purpose of the training

It is aimed that the participants have information on the following subjects,

·       Purpose and Importance of Method Validation

·       Method Performance Parameters (Selectivity, LOD / LOQ, Accuracy, Precision etc.)

·       Calculation of Validation Data and Evaluation of Appropriateness (Using F test, t-test, ANOVA etc.)

Who can participate?

·       People who want to develop and improve themselves who will be involved in method validation and validation studies can participate in this training.

·       Validation training is a general training and does not include information on specific test areas.

Prerequisite

·       Having received TS EN ISO / IEC 17025 - General Conditions for the Qualification of Testing and Calibration Laboratories standard training or having basic knowledge

·       It is considered that it would be beneficial for the participants to have basic knowledge of mathematics and statistics.

·       Participants are required to bring their personal computers.

The maximum number of participants is 20 people. Limiting the number of participants in this type of training is important for the efficiency of the training.

 Introduction

In "Traceability of Measurements and Measurement Uncertainty Training" for calibration laboratories, it is intended for the determination, use and reporting of ‘measurement uncertainty, which is mandatory in accordance with TS EN ISO / IEC 17025 - General Requirements for the Competence of Testing and Calibration Laboratories, by calibration laboratories planning to be accredited or accredited for the methods within the scope of service. In addition, basic theoretical and practical information is given on the traceability of measurements to national and international measurement standards.

Purpose of the training

·       To inform the organizations that have applied or accredited for accreditation at a basic level regarding the determination, use and reporting of measurement uncertainty in the methods within the scope of accreditation,

·       To inform the participants at the basic level about the traceability of measurements to national and international measurement standards,

·       Providing information on the relevant national and international policies and procedures on the traceability of measurements and measurement uncertainty,

·       It is aimed to include theoretical and practical applications in metrological traceability, SI Units and calculation of measurement uncertainty for testing laboratories.

Who can participate?

Anyone who has applied for accreditation or who takes part in the determination, use and reporting of measurement uncertainty of accredited calibration laboratories can participate in the training.

Measurement uncertainty training is a general training and does not include information on measurement uncertainty in specific test areas.

Prerequisite

·       Having received TS EN ISO / IEC 17025 - General Conditions for the Qualification of Testing and Calibration Laboratories standard training or having basic knowledge. (It needs to be evaluated by the relevant Directorate)

Training duration: 2 Days

Training fee: 3400 TL + VAT 

The maximum number of participants is 20 people. Limiting the number of participants in this type of training is important for the efficiency of the training.

 Introduction

In accordance with the TS EN ISO / IEC 17025 standard internal audit article, laboratories are required to operate an internal audit mechanism that meets the requirements of the standard. This training will provide a suitable environment in terms of interpreting the relevant articles of the standard in accordance with its purpose and evaluating the issue with different perspectives and examples for an effective internal audit.

Purpose of the training

To provide information on how an internal audit that meets the expectations of the TS EN ISO / IEC 17025 standard will be and to raise awareness about the contribution of the internal audit to quality management.

Who can participate?

Anyone who takes part in TS EN ISO / IEC 17025 quality management and laboratory applications can participate.

Prerequisite

Having sufficient knowledge and experience about TS EN ISO / IEC 17025 is very important for the effectiveness of the training. Those who do not have sufficient knowledge and experience about the standard are not recommended to participate.

The maximum number of participants is 20 people. Limiting the number of participants in this type of training is important for the efficiency of the training.

 

 

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 Introduction

TS EN ISO / IEC 17025 Standard, which is the basic document used by the Turkish Accreditation Agency (TÜRKAK) for the accreditation of test and calibration laboratories, is an international standard that includes general requirements for the competence of test and calibration laboratories. The articles of the TS EN ISO / IEC 17025 standard reveal the general conditions of a laboratory’s quality management system and technical competence. The purpose of this 3-day training is to give the participants an accurate perspective on the interpretation of the standard.

Purpose of the training

·       to give participants an accurate perspective on TS EN ISO / IEC 17025 Standard,

·       To contribute to the work of laboratories by interpreting the management and technical conditions clauses that form the basis of the standard,

·       It is aimed to provide the participants with basic information about TURKAK’s role in accreditation of test and calibration laboratories and accreditation processes.

Who can participate?

·       Laboratory managers,

·       Quality managers,

·       Calibration and test laboratory employees,

·       Anyone who wants to improve himself / herself regarding the General Conditions Standard for the Competence of Testing and Calibration Laboratories of TS EN ISO / IEC 17025 can participate in this training.

Prerequisite

There is no precondition to participate in this training. Participants are recommended to have the TS EN ISO / IEC 17025 Standard.

The maximum number of participants is 20 people. Limiting the number of participants in this type of training is important for the efficiency of the training.

Introduction

TÜRKAK bases its accreditation assessments for inspection bodies on the globally recognized standard “TS EN ISO/IEC 17020:2012 - Conformity assessment - Requirements for the operation of various types of inspection bodies.” The training program, “TS EN ISO/IEC 17020:2012 Standard Training,” provides insights into the interpretation of the standard, its practical implementation, and the policies followed during the accreditation process of inspection bodies.

Objective

The purpose of this training is to inform participants about the requirements set forth by TS EN ISO/IEC 17020:2012 and TÜRKAK’s documents for the accreditation of inspection bodies. As Turkey's sole authority authorized to issue accreditation certificates, TÜRKAK ensures participants receive expert knowledge directly from the most competent source in the field of inspection accreditation.

Training Content

• General information about accreditation and TÜRKAK’s activities
• Interpretation of TS EN ISO/IEC 17020:2012
• General approaches to the accreditation of inspection bodies
• Accreditation process for inspection bodies
• Practical group exercises

Who Can Attend

The training is open to managers, quality management personnel, technicians, and relevant staff from inspection bodies affiliated with:

• Public and private universities
• Public institutions
• Private companies and individuals

Additionally, anyone wishing to enhance their knowledge of the TS EN ISO/IEC 17020:2012 standard is encouraged to attend.

Prerequisites

• No prerequisites are required.
• Participants are advised to bring their own laptops for practical applications and to procure a copy of the TS EN ISO/IEC 17020:2012 standard.

Training Details

• Duration: 2 Days
• Fee: 3400 TL + VAT
• Maximum Participants: 20

Limiting the number of participants ensures the effectiveness of the training.

Important Notes:

• Training fees must be paid via credit card during the e-portal application process. EFT or wire transfer payments to TÜRKAK’s bank accounts will not be accepted.

This program provides an excellent opportunity to gain expert knowledge directly from TÜRKAK, enhancing competencies in inspection body accreditation.