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Clinical Trial Management & support services

Overview

Headquartered in Australia, Akesa specialises in supplying pharmaceutical products for preclinical and phase I-IV clinical trials, globally, working alongside sponsors, CROs, research institutions, clinical trial sites and CDMOs to design and project manage supply solutions.

Clinical trial products and supplies
Akesa understands the challenges faced by sponsors in sourcing registered pharmaceuticals for clinical trials. Our years of experience, market knowledge, consultative service approach and supplier means we can secure products from validated suppliers and directly from manufacturers, including:
• comparator products
• combination therapies
• concomitant or standard of care medication
• rescue Medication
• sample for analysis

Our adaptive approach can support the unique requirements of each clinical trial including large volumes, long expiries, and access to product documentation.

Clinical trial services
Akesa’s clinical trial services provide customers with a complete end-to-end solution for their clinical trial supply projects – from project management, forecasting and planning, to product sourcing, labelling, storage and distribution direct to site and to patient.
Akesa’s on-demand clinical trial site sourcing solutions are designed to simplify and streamline the supply of clinical trial medicines for the sponsor, pharmacy and clinical trial site. This ensures just-in-time access for patients, minimising product wastage, increasing accountability of standard of care medications and alleviating administrative burdens on hospital pharmacies.
Akesa’s managed access programs are crucial in bridging the healthcare access gap between clinical trials and market availability. Akesa manages post-trial supply requirements or commercial access programs that are delivered through a central PBS-licensed pharmacy with national coverage.

Delegates

Portrait-Karen-Montgomery-Douglas-1×1-1.jpg
Karen Montgomery-Douglas
Commercial Development Manager