Call for Speaker Proposals
第3屆
Personalized Diagnostics
-個別化診斷學會-
對臨床醫學的影響
2月21日∼23日
個別化診斷若能作臨床應用，就能把患者分階層、以分子水平來分類疾病，判斷發生的可能性，提出能最佳的治療法。這樣的方法不僅有助於削減醫療費和改善治療，亦能成為實現消費者以自己意思進入醫療資訊環境的力量。此學會選擇有助於研究與臨床應用的技術，亦聚焦於將新的研究成果轉換成有效商務模式的方法。
Who Should Attend: VPs, Directors, Managers, CEOs, CSOs, Professors and Scientists from Large Pharma, Biotechs and Academia working in fields such as Diagnostics, Business Development, R&D, Chemistry, Clinical Research, in vitro Diagnostics, Personalized Healthcare, Process Development, and Oncology.
Topics will include, but are not limited to:
- Third generation sequencing as a clinical tool
- Integrating molecular and cell-based diagnostics
- Leveraging epigenetics, gene mutation analysis, and gene expression assays
- Using proteomics as a diagnostic tool
- Mass spec to find and monitor biomarkers in blood
- NGS for mitochondrial disease diagnostics
- Assembling gene panels
- NGS data management
- RNA sequencing
The deadline for submission is July 29, 2011.
All proposals are subject to review by the Scientific Advisory Committee to ensure the highest quality of the conference program. Please note that due to limited speaking slots, preference is given to pharmaceutical and biotech companies, regulators and those from academia. Additionally, vendors/consultants who provide products and services to these biopharmaceutical companies are offered opportunities for podium presentation slots based on a variety of Corporate Sponsorships.
