Clinical Logistics & Regulatory Support

Nadarra Health partners with Australian and international organisations to deliver end-to-end clinical logistics and regulatory support for investigational and early-phase products within Australia. We work with overseas sponsors to coordinate and manage importation, compliant storage, controlled distribution to clinical sites, and ongoing supply oversight, ensuring continuity throughout the study lifecycle.

Operating from our licensed facility in Melbourne, we provide secure storage for Schedule 4, 8 and 9 products, including controlled cannabinoids, supported by a robust Quality Management System and electronic inventory control platform. Our team brings over 30 years of combined experience in GMP environments and the supply of clinical products to hospital and patient sites, with established processes for chain-of-custody integrity, temperature control and reconciliation.

Beyond logistics, Nadarra offers integrated GMP advisory, audit support, clinical management coordination and regulatory liaison, including facilitation of discussions with the TGA where appropriate. We assist sponsors in preparing compliant documentation, maintaining inspection readiness and managing deviations including structured product return and recall processes where required.

Our approach is operationally focused and risk-based, designed to provide sponsors with confidence that clinical product supply in Australia is secure, compliant, and professionally managed from importation through to site delivery and close-out.

For organisations seeking a capable Australian partner to support clinical supply and regulatory coordination, we welcome confidential discussions.­