500+ Systems Validated
ERP, LIMS, QMS, MES, SCADA, Cloud Applications, Spreadsheets, Custom Apps
15+ Pharma, Biotech & Medical Device Clients Served
Global Life Sciences Clients
1000+ GxP Processes Validated
Quality, Manufacturing, Lab, Packaging, Compliance, R&D
150+ Medical Devices & Digital Health Systems Validated
Class I, II, III devices, Embedded Systems
Our Vision
Trust, Compliance, Delivered
Training Services
All training activities, courses, webinars, workshops, are designed to provide a practical and experience-based approach.
Audit Library
Explore our extensive GMP audit library to see the range and scope of reports we have in stock, join a live audit, or commission a bespoke audit.
Regulatory
As you review and strengthen GMP compliance, we can team up for specific projects like regulatory filings & submissions up to standard.
About Us – QFORCE Pharma Consulting LLP
Computer System Validation, GxP compliance, and audit-ready documentation.
QFORCE Pharma Consulting LLP brings over 30 years of proven Quality Assurance excellence from highly regulated pharmaceutical and biotech environments.
Founded by a seasoned QA leader with recognized authority in enforcing quality and compliance, QFORCE has built a strong reputation for Computer System Validation, GxP compliance, and audit-ready documentation.
Our expertise spans Pharma, Biotech, and Medical Devices, ensuring every system, process, and digital platform meets the highest global regulatory standards.
Now part of PRIMUS Techsystems, QFORCE combines domain depth with modern digital capabilities to deliver reliable, compliant, and scalable validation solutions.
We remain committed to strengthening patient safety, operational integrity, and end-to-end compliance across the life sciences value chain.
