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  Clinical Pharmacology
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QA / QC
We have a robust QA/QC system that independently monitors Clinical, Bioanalytical, Pk & Statistical activities to ensure compliance to Protocol, SOPs, GCP, GLP and other regulations

Our QA Team is responsible for the following:

  • Coordinate all regulatory inspections and applicable client audits
  • Control revisions of Standard Operating Procedures and applicable forms
  • Conduct annual internal System audits
  • Monitor study for protocol and SOP compliance
  • Audit data to ensure that it accurately reflects the raw & source data
  • Consistently meeting client’s expectation for quality and timelines of project.



 
   
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