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Synchron has a detailed set of Standard
Operating Procedure for the clinical and analytical facilities. Our
Quality Assurance team operates independently and reports directly
to the management. All our QA staff is well trained to audit various
activities of Phase I - Phase IV clinical trials.
GCP audit
Investigator site audit
Data base audit
Final report audit
Laboratory audit
System audit
SOP writing and reviewing
In house files' audit |
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