Clinical Trial Supply East Asia 2018
Dec. 5, 2018 – Dec. 6, 2018 • Seoul, South KoreaRegister
Arena International is thrilled to announce that the 4th Clinical Trial Supply East Asia conference is returning to Seoul on the 5th - 6th December 2018.
This conference will address how companies can effectively streamline clinical supply processes to ensure timely and cost-effective clinical studies and be responsive to industry trends to enable early market penetration. This conference offers a great opportunity for delegates to network with industry professionals and service providers, as well as attending insightful lectures from industry experts within the East Asia region.
If you would like to attend this year’s event, register today and quote MK-BPMEID
- Pinpointing difficulties in the transportation of Cell & Gene therapy products (Yoonjung Cho, Clinical Trial Manager, Director - SCM Lifescience)
- Key Factors of success in preparing cGMP inspection according to quality by design development (Chih-Ping Liu, Vice President, TTY Biopharma Company)
- Establishing forecasting best practice: minimizing cost associated with your supply chain through waste minimization (DaeMan Moon, Team Leader, Development Supply Chain - Celltrion)
- Speed, Quality & Cost - Why you should be conducting your clinical trials in Australia (Bev Thomas, GM Operations, PCI Clinical Services)