Akesa stands as your steadfast partner, dedicated to advancing pharmaceutical innovation. With global expertise spanning early-phase trials to aiding Clinical Research Organisations (CROs) and Contract Development and Manufacturing Organisations (CDMOs), we specialise in procuring vital comparator drugs and streamlining supply logistics.
As Asia-Pacific specialists with a global footprint, we bring over a decade of experience and a profound understanding of pharmaceutical development. Our commitment to excellence ensures we are your strategic guide, navigating the intricacies of drug discovery. Embrace Akesa’s comprehensive support and industry insight, propelling you toward transformative healthcare breakthroughs.
Early Phase Trials – BrinGing Your Drug to market
At Akesa, we provide comprehensive early phase drug trial support tailored to sponsors’ and patients’ unique needs. Our services are designed for efficiency, streamlining the trial process to ensure smooth operations.
We are committed to collaborating with you to develop a customised strategic approach for your early phase trials. We understand that a reliable supply chain is pivotal for trial success, especially in early phases. We recognise the significance of sourcing comparator medications and work closely with you to devise a strategy that guarantees a seamless and consistent supply of these essential components.
Our goal is to empower you with a competitive edge, allowing you to execute your early phase trial with confidence and precision. Take the first step towards early phase trial success with Akesa and secure your path to market.
Your Collaborative Partner for CRO Clinical Trials
Akesa, the Asia-Pacific specialists with a global reach, is the trusted partner for leading Clinical Research Organisations (CROs), expediting and streamlining your Sponsor’s clinical trials. Our dedicated team serves as the crucial point of contact for your strategic planning, feasibility, and operations teams, providing market insights and product access strategies to empower your team with vital information for robust project planning.
We oversee the supply and procurement of comparator and combination therapies, rescue medication, and analysis samples, allowing you to focus on the essential task of executing successful trials. By engaging our project management team at the outset of your Sponsor’s clinical trial, we ensure timely and budget-friendly trial completion. Akesa stands as your strategic ally in achieving clinical trial success. Elevate your CRO clinical trials with Akesa to expedite and streamline your trials for timely success.
Your Strategic Partner for CDMOs
Akesa is the esteemed partner of prominent global Contract Development and Manufacturing Organisations (CDMOs), specialising in the procurement of essential comparator drugs crucial for your Sponsor’s clinical trials.
As a trusted sourcing expert with a remarkable track record of over 1,000 clinical trials, 50% of which are phase 3 global trials, we possess the experience and capability required to meet the rigorous demands of CDMOs.
The Asia-Pacific Leader with Global Reach
With a decade of experience and headquarters in Australia and operations in Singapore, Akesa stands as the foremost clinical trial supply specialist in the Asia-Pacific region. Our direct associations with manufacturers and an extensive global network of reliable suppliers spanning Australia & New Zealand, Singapore, Japan, Korea, the United States, Europe, and the United Kingdom enable us to offer invaluable market insights and sourcing strategies during the planning phase, allowing us to proactively identify challenges and minimise risks. Unlock the potential of your CDMO trials with Akesa, your trusted partner for essential comparator drugs.
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Partner with Akesa Clinical Trial Supply for a reliable and consistent supply of pharmaceutical products, and dedicated support for your clinical trial. Let us help you navigate the complexities of commercial supply, mitigate potential risks, and ensure that your trial runs smoothly from start to finish. Contact us today to learn how we can support your drug development journey.
