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PharmaVision

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General Requirements for the Competence of Testing and Calibration Laboratories

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TS EN ISO/IEC 17025 Laboratory Accreditation CertificateThis standard includes all the requirements for laboratories, which aim to demonstrate that they are employing a management system, are technically qualified and are able to produce valid technical results.

Employing this standard enables the creation of cooperation between laboratories and other institutions, mutual exchange of know-how and experience and harmonization of standards and procedures.

PharmaVision Qualification, Validation, Adjustment-Control Calibration Laboratory has decided to implement the quality system in line with TS EN ISO/IEC 17025 standard and with the support of the executive management has applied this system starting in 2008, in order to use internationally-accepted procedures, increase the reliability of experimental services and improve in performance.

In order to meet all the requirements of TS EN ISO/IEC 17025 standards, documented procedures have been established within the institution with the aim of increasing the customer satisfaction resulting from high quality and reliable experimental services.
 

 

 PHARMAVISION QUALIFICATION, VALIDATION, ADJUSTMENT-CONTROL, CALIBRATION LABORATORY QUALITY POLICY

In accordance with our qualification, validation, adjustment-control and calibration laboratory quality policy;

  • Providing testing services, fully compliant with legal requirements and in line with national/international standards or testing methods wtihin the scope of Good Occupational Technical Practices in the most timely manner,
  • Not allowing commercial, financial or other pressures to endanger impartiality,
  • Taking necessary precautions for the confidentiality of internal customer information in laboratory activities,
  • Conducting tests in accordance with policies and procedures fulfilling the requirements of current TS EN ISO/IEC 17025 standard and adhering to principles of independence, honesty and reliability build the basis of our actions.

Our aim is;

To apply the principles of the quality management system with the commitment of all our associates and prevent any possible factor which may have a negative effect on test results.

Our targets are;

To benefit from the expertise of our specialist team while using proper test equipment as given in test instructions and standards; fulfil the received test requirements in the highest percentage possible; conduct and result the tests in the most accurate way by using necessary reference standards, provide a sustained and high level of test quality, prevent eliminate any possible customer complaints to maintain full customer satisfaction. 

We hereby declare that, we will comply with the requirements of TS EN ISO/IEC 17025 standard and provide all necessary resources for the sustainable development of the quality management system.

Dr.Ünsal Hekiman                                                                                         
Chairman of the Board/General Manager

 
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