Cromos Pharma performs independent audits of sites and facilities followed by a formal detailed report with a comprehensive description of all findings noted. All activities are performed in accordance with appropriate SOPs and Working Instructions. Our certified auditors perform a wide range of independent audits that include:

  • Clinical site GCP audits
  • Documentary audits for Trial Master File
  • System Vendor Audits
  • Regulatory Inspection and Sponsor’s audit readiness check

Cromos Pharma Quality department provide consultancy services for Quality Management system development, implementation and maintenance, including Quality Management System for investigational sites.

All audits are followed by a detailed report including the description of findings and possible corrective and preventive actions.

If you are interested in independent audit of your site/facility/vendor services, please contact our Quality Director.