At the heart of MedPharm’s development and manufacturing excellence is a deeply embedded Quality Assurance (QA) culture. Our QA team operates independently yet collaboratively across functions to ensure all processes are executed correctly, documented thoroughly, and reviewed against the most current standards.
We don’t see QA as a checkpoint. We see it as a strategic partner in every project.
Batch Release
Batch Record Review and Product Release
GMP-compliant processes for clinical trial material and commercial batch disposition
Inspections
Audit Readiness and Inspection Hosting
Internal audits, third-party audits, and health authority inspections managed with full transparency
Documentation
Document Control and SOP Management
Cloud based eQMS ensuring document control and periodic review execution
CAPA
Deviation and CAPA Management
Immediate investigation, risk assessment, and resolution of any non-conformance
Change Control
Change Control Oversight
Evaluation and QA approval of process, equipment, or material changes
Suppliers
Supplier Qualification and Oversight
Ensuring raw materials, components, and vendors meet MedPharm’s quality expectations
