Your Trusted Partners for Quality Assurance and Regulatory Services…
Some of our Recent Projects :
  • GCP audit of the CRO and the investigator sites for leading European medical device company. Critical findings led the termination of CRO.
  • GCP audit of the leading global CRO.
  • ‘For Cause’ Audit on behalf of big pharma of the global investigator site, prior to USFDA inspection.
  • Preparation of end-to-end SOPs for Clinical Data Management and Biostatistics of the leading CRO conducing global studies, including GCP Training for regulatory inspection preparedness.
  • Over 100 GCP Training Programs for CROs, Investigator Sites and Pharmaceutical companies.
  • IMP Depot audit.
  • Pharmacovigilance QA SOPs preparation for the leading CRO.
  • Pharmacovigilance LPVRP SOPs preparation for Asia Pacific Region.
  • GMP Audit of Indian pharma manufacturing facility on behalf of leading global NGO.
  • Ethics Committee Formation, Regulatory Compliances and Training.
  • Pre inspection GLP trainings.
What's New
CRQA is looking for
qualified and Independent
Pharmacvovigilance Auditor
- experience essential in
Pharmacovigilance Audits.
Interested Professionals
may apply to bd@crqa.in
CRQA is looking for
qualified and Independent
Pharmacvovigilance Auditor
- experience essential in
Pharmacovigilance Audits.
Interested Professionals
may apply to bd@crqa.in
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