Quality Statement

Quality is defined as a measure of excellence or a state of being free from any defects. We have re-defined this statement and believe that quality results from the combination of perception and expectation. The feeling of high quality occurs when perception exceeds expectation
 

Clearsynth is accredited to ISO 45001:2018, ISO 9001:2015, ISO 14001:2015, ISO 17034:2016, ISO/IEC 17025:2017 along with US FDA registration & DSIR recognition. Our management and employees take pride in our Quality System and fully support the implementation, monitoring and continuous improvement of our processes.


We believe in doing it right even when no one is looking.



Quality Checks

  • On-Going Quality check programs for understanding of chemical reaction
  • Monthly internal meetings for formal failure analysis of any non-conformances.
  • Constant review of procedures and adapting more qualitative approach
certificates

ISO 45001:2018

Certificate for Occupational Health & Safety Management System of Clearsynth Labs Research Centre.

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certificates

ISO 9001:2015

Certificate for Quality Management System of Clearsynth Labs Research Center.

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certificates

ISO 14001:2015

Certificate of Environmental Management System of Clearsynth Labs Research Center.

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certificates

ISO 17034:2016

Certificate for Accreditation Commission for Conformity Assessment Bodies of Clearsynth LAbs Research Center.

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certificates

ISO/IEC 17025:2017

Certificate for Accreditation Commission for Conformity Assessment Bodies of Clearsynth Labs Research Center.

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certificates

DSIR Recognition

Clearsynth Labs Ltd. is registered with the U.S. Food and Drug Administration for the statutory filing period applicable to the U.S.

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