At Clearsynth, we are reimagining research At each level of our business we ensure we adhere to strict quality controls
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

ISO 45001:2018
Certificate for Occupational Health & Safety Management System of Clearsynth Labs Research
Centre.
[View
Certificate]

ISO 9001:2015
Certificate for Quality Management System of Clearsynth Labs Research Center.
[View
Certificate]

ISO 14001:2015
Certificate of Environmental Management System of Clearsynth Labs Research Center.
[View
Certificate]

ISO 17034:2016
Certificate for Accreditation Commission for Conformity Assessment Bodies of Clearsynth LAbs Research
Center.
[View Certificate]

ISO/IEC 17025:2017
Certificate for Accreditation Commission for Conformity Assessment Bodies of Clearsynth Labs Research
Center.
[View Certificate]

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.
[View Certificate]
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