Quality Analysis

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Quality Assurance

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
  • Vendor Audits