Core Service
Quality Assurance
How is Quality Assurance Established for Global Access and Clinical Supply Chains?
An integrated quality assurance framework is established through a globally aligned, audit ready Quality Management System (QMS) that governs all regulated activities across access and clinical supply chains. This includes validated systems, controlled procedures, and documented oversight to ensure GDP, GMP and broader GxP compliance, traceability and inspection readiness.
At Tanner Pharma, quality assurance is delivered through a global QMS and continuous operational oversight.
Tanner manages supplier and customer qualification, quality assurance agreements, change controls, deviations, CAPAs and ongoing quality monitoring to protect execution integrity, regulatory compliance and product quality.
Our Quality Framework
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Validated eQMS platform with integrated Learning Management System
Globally harmonized and compliant procedures
Training governance and internal audit programs
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Proactive risk identification and mitigation
Control, mitigation, and communication
Partner qualification and performance monitoring
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Quality assurance continuity from early clinical supply through post-approval access programs
Oversight supporting consistent quality standards across global operations
Facilitates innovation and continuous improvement
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Structured quality metrics and leadership reporting
Inspection-ready documentation and workflows
3rd party certifications for compliance
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Workflow automation and document control
Data integrity controls and security
Comprehensive solution for DSCSA and FMD compliance
Licenses & Authorizations
Tanner Pharma maintains the licenses, certifications and regulatory authorizations required to operate as a compliant global access and clinical trial services partner. These credentials support the compliant sourcing, storage, packaging, import, export and distribution of medical products in accordance with global regulatory and quality expectations.
