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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 Record Review and Product Release
GMP-compliant processes for clinical trial material and commercial batch certification
Audit Readiness & Inspection Hosting
Internal audits, third-party audits, and health authority inspections managed with full transparency
Document Control & SOP Management
Rigorous version control and review cycles for procedural accuracy and traceability
Deviation and CAPA Management
Immediate investigation, risk assessment, and resolution of any non-conformance
Change Control Oversight
Evaluation and QA approval of any process, equipment, or material changes
Supplier Qualification and Oversight
Ensure raw materials, components, and vendors meet MedPharm’s quality expectations
