Akesa is the trusted partner of leading global Contract Development and Manufacturing Organisations (CDMOs), specialising in sourcing comparator drugs essential for your Sponsors clinical trials. A trusted sourcing specialist with over 1000 clinical trials to our name, 50% of which are phase 3 global trials, we have the experience and capability to meet the rigorous demands of CDMO’s.
The Asia-Pacific Specialist with Global Influence
With 10 years of experience, headquartered Australia and Singapore, Akesa is the leading clinical trial supply specialist in the Asia Pacific region. We have direct relationships with manufacturers and a global network of trusted suppliers in:
- Australia & New Zealand
- Singapore
- Japan
- Korea
- United States
- Europe
- United Kingdom
This network equips us to provide market intelligence and sourcing strategies in the planning stage and allows us to identify challenges early and reduce risk.
Documentation and Product Procurement
Understanding the needs of a CDMO, Akesa can provide documentation on a case-by-case basis. This includes:
- Certificate of analysis, (CoA)
- Equivalency documents i.e. AU/EU, AU/USA, AU/CHN
- Logistics data
- Country of Origin
We also procure products tailored to specific customer requirements, be it multiple batches, dedicated manufacturing runs, or specific expiry dates.
Committed to Quality and Compliance
Quality management is at the core of what we do. Our Quality Management System (QMS) is designed to comply with the EU Good Distribution Practice (GDP) and backed by ISO9001 Certification. We have a dedicated quality team and an ISO9001 accredited QMS to ensure that we meet the highest standards. Akesa also undergoes and successfully passes qualification audits conducted by our customers, making us a reliable partner for your CDMO needs.
Let’s connect!
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.
