Advanced Toxicology Analysis Laboratory

The aim of our laboratory is to contribute in the prevention and treatment of drug abuse by identifying, designating and analyzing toxic and addictive substances, integrate EU rules, improve cooperation, provide institutional developments and improve physical and technical infrastructure.

In our laboratory, quantitative analysis of toxic and addictive substances (opiate, amphetamine group, cannabis, synthetic cannabinoids, alcohol, cocaine) are performed in urine by Waters XEVO TQD Ultra-performance liquid chromatography, coupled with tandem mass spectrometry (UPLC-MS/MS) device.

Our laboratory has TS/EN ISO17025 Accreditation and CAP External Quality Control Certificate. In this context, each test is performed according to the TS/EN ISO17025 rules in our laboratory. Additionally, testing is performed with external quality control urines sent by CAP (The College of American Pathologists) every 3 months.

Our laboratory ensures systematic analytical accuracy and possible random errors to be within acceptable limits.

When the samples’ waiting time expires, they are delivered to the medical waste with a written report for disposal in accordance with the legal regulations.

Our Toxicology Laboratory is in the National Media Spotlight!

Cihaz Cinsi

Adedi

Refrigerator (+4)

1 Piece

UPLC-MS/MS - Waters

1 Piece

Waters Acquity Plus UPLC Binary Solvent Manager

1 Piece

Waters Acquity Plus UPLC Sample Manager FTN

1 Piece

Waters Xevo TQD

1 Piece

Heidolph Vortex

1 Piece

Hettich Rotofix Centrifuge

1 Piece

Mettler Toledo Al 104 Scale

1 Piece

OHAUS Discovery DV215 CD Scale

1 Piece

Eppendorf Micro Pipet Set

2 Piece

Generator LCMS 6410

1 Piece

Binder drying oven RL 10

1 Piece

Heidolph Multivortex

1 Piece

ELGA Purelab Deiyonized water device

1 Piece

Bandelin Sonicator

1 Piece

IKA RH Basic 2 Heated Magnetic Stirrer

1 Piece

Millipore water filtration system

1 Piece

Fume Cupboard

1 Piece

Testo Heat and Humidiometer

1 Piece

Freezer (-70)

1 Piece

Freezer (-20)

2 Piece

Uğur ATİK Uğur ATİK, Ph.D
Professor of Biochemistry
 
VSHS / Medical Laboratory
Prof. Uğur Atik is a Clinical Biochemist. Graduated from Faculty of Pharmacy at Ankara University in 1968. He took his Ph.D. degree at Gulhane Military Medical Academy (GATA), Faculty of Medicine, Department of Biochemistry in 1980 .Has worked at the ... [ » ]
Uğur ATİK / (0216) 400 2222 - : 2994
Selma ÖZİLHAN Selma ÖZİLHAN,  
Advanced Toxicology Laboratory Analysis In-Charge
Ms. Özilhan was Born in 1954 in Ordu. She graduated from the Ankara High School for Girls. She completed her graduate studies at the Faculty of Pharmacy of Hacettepe University and holds an M.Sc. degree in the field of Bağlantıpharmacognosy from Gazi ... [ » ]
Selma ÖZİLHAN / (0216) 400 2222 - : 2996
Fadime CANBOLAT Fadime CANBOLAT, CV
Lecturer Fadime Canbolat was born in İstanbul in 1982. She graduated from Selçuk University Faculty of Science, Chemistry Department in 2004. In 2007, Selçuk University Institute of Health  Sciences has completed a master's degree in Pharmacolog ... [ » ]
Fadime CANBOLAT / (0216) 400 22 22 - : 2997
Aykut Kul Aykut Kul,  
[...]
Aykut Kul / (0216) 400 2222 - : 2998
Murat ÖZDEMİR Murat ÖZDEMİR,  
[...]
Murat ÖZDEMİR / (0216) 400 2222

Certificate of Accreditation

What Is Accreditation?
Accreditation is a quality infrastructure created in order to support the reliability and validity of conformity verification documents (test and examination reports, calibration certificates, management system documentation, product documentation, personnel documents, etc.) prepared by conformity assessment bodies. Accreditation of conformity assessment bodies is carried out on the basis of relevant industry-specific requirements and requirements designated in guidelines by regional or international accreditation organizations, worldwide accepted qualification criteria on international standards for the relevant conformity assessment bodies.   
TS EN ISO/IEC 17025 Competence of Testing and Calibration Laboratories
Accreditation organizations recognizing the technical competence of the experimental laboratories shall base the accreditation of these laboratories on ISO/IEC 17025.
TS EN ISO/IEC 17025 Standard includes general requirements for the competence of testing and calibration laboratories, as well as a laboratory's technical proficiency and ability to produce technically accurate and reliable results. Through the introduction of a single standard as an indicator of laboratory competence at the international level, it is aimed testing and calibration laboratories anywhere in the world to compete with each other at the same level. Because of the international validity of the test reports or calibration certificates, this condition provides a wider market, in other words a wider customer base for the laboratory accredited according to the ISO/IEC 17025 standard.
Many countries in the world determine the technical competence of laboratories with the help of the accreditation systems. There may be one or more accreditation organizations in a country. In our country, Turkish Accreditation Organization (TÜRKAK) is commissioned with Article Nr 4457 to accredit laboratories. Today, accreditation of testing laboratories is based on the TS EN ISO/IEC 17025 Standard. These standards are accepted worldwide. The items of the aforementioned standard lay out the general conditions of a laboratory's quality management system and technical competence.
According to this standard, laboratories accredited are inspected periodically by the accreditation organization, and the continuation of accreditation is decided according to the result.
For the continuation of accreditation, laboratories have to participate in the comparison and proficiency test programs related to the accreditation, and to receive successful results.
Key principles for ISO17025:

  • Internal Quality Control Schemes
  • Competence tests or inter-laboratory comparison tests
  • Operation instructions or Standard Operating Procedures (SOPs)
  • The use of standard reference materials or quality control in the laboratory by using sub-references
  • The use of appropriately maintained and calibrated instruments
  • Validated methods
  • Reporting of measurement uncertainty
  • Quality staff
  • Recording and reporting

Although it is not compulsory to be accredited according to TS EN ISO/IEC 17025:2005 Standard, it is impossible for laboratories that are not accredited; i.e. laboratories that are not able to show that they produce valid technical results; to be accepted as reliable and to compete commercially with laboratories accredited.  
ACCREDITATION proves that a laboratory has technical competence and produce valid technical results both nationally and internationally. 
The requirements of the ISO 17025 standard consist of two main sections:

  1. Management Requirements: Describe the conditions necessary for the execution of a quality system.
    In this context
    • Organization
    • Management system
    • Document control
    • Review of requests, tenders and contracts
    • Subcontracting of tests and calibrations
    • Purchasing services and supplies
    • Service to the customer
    • Complaints
    • Control of nonconforming testing and/or calibration work
    • Improvement
    • Corrective action
    • Preventive action
    • Control of records
    • Internal audits
    • Management reviews
  2. Technical Requirements: It includes the requirements for staff competence, methodologies, equipment testing and calibration, and test methods 
    In this context:
    • Personnel
    • Accommodation and environmental conditions
    • Test and calibration methods and method validation
    • Equipment
    • Measurement traceability
    • Sampling
    • Handling of test and calibration items
    • Assuring the quality of the test and calibration results
    • Reporting the results

Advantages of ISO17025:

  1. Through the introduction of a single standard as an indicator of laboratory competence at the international level, it is aimed testing and calibration laboratories anywhere in the world to compete with each other at the same level.
  2. A product or service with a compliance certificate issued by a compliance assessment authority inculcates confidence that the applicable requirements for this product or service are provided.
  3. Through this systematic, accreditation contributes to the removal of technical barriers in trade
  4. Because of the international validity of the test reports or calibration certificates, this condition provides a wider market, in other words a wider customer base for the laboratory accredited according to the ISO/IEC 17025 standard.