PharmEng Technology

Comprehensive GxP supplier audits, data integrity assessments, and regulatory inspection readiness for biotechnology firms.

PharmEng Technology

Quality Auditing & Inspections

Global GxP Auditing, Facility Commissioning & Quality Oversight

Toronto, ON, Canada

Company Overview

PharmEng Technology offers full-lifecycle quality engineering, commissioning, and third-party compliance auditing for pharmaceutical and biomanufacturing facilities.

They deliver global supplier qualification audits across raw material producers, contract manufacturers, and testing laboratories, verifying adherence to cGMP and PIC/S standards.

PharmEng also assists manufacturing sites with computerized system validation, data integrity gap analyses, and pre-approval inspection preparedness.