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Point-of-Care Testing
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°³¹ß±â°£ÀÇ ´ÜÃà°ú °æºñÀý°¨¿¡ µû¶ó ÀÓ»ó½ÃÇèÀ» È¿À²È­ÇÒ Çʿ伺ÀÌ Ä¿Áö´Â °¡¿îµ¥ ȯÀÚ¸¦ °èÃþÈ­Çϱâ À§ÇØ Point of Care °Ë»ç¸¦ ÀÌ¿ëÇÏ´Â ÄÉÀ̽º°¡ Áõ°¡Çϰí ÀÖ½À´Ï´Ù. ÀÌ ½ÉÆ÷Áö¾ö¿¡¼­´Â Point of Care Áø´ÜÀÇ ±â¼ú ¹× µ¿ÇâÀ» ´Ù·ç¸ç ½Å¾à °³¹ß ºÐ¾ßÀÇ °¢Á¾ ¿ëµµ¿¡ ´ëÇÑ ÀûÇÕ¼ºÀ» °ËÅäÇϰí, Áø´Ü ¼­ºñ½º ÇÁ·Î¹ÙÀÌ´õ ¹× Á¦¾àȸ»ç ¾çÃø¿¡ ´ëÇÑ ºñÁö´Ï½º ±âȸ¸¦ ¸íÈ®È÷ ÇÕ´Ï´Ù. ¶ÇÇÑ µ¿¹ÝÁø´ÜÀÇ µµÀÔ °ü·Ã ¹®Á¦ ¹× Point of Care °Ë»ç°¡ À¯È¿ÇÑ ÅøÀÎ ÀÌÀ¯ µîµµ Á¦½ÃµÉ ¿¹Á¤ÀÔ´Ï´Ù.

Who Should Attend: VPs, Directors, Managers, CEOs, CSOs, Professors and Scientists from Large Pharma, Biotechs and Academia working in fields such as Diagnostics, Pathology, Infectious Diseases, R&D, Product Development, and Biotechnology.

Topics will include, but are not limited to:

  • Technologies and trends in point-of-care diagnostics
  • Deciding which companion diagnostic test to use
  • Implementing companion diagnostics
  • Partnering with a point-of-care diagnostic developer
  • Deciding on criteria for selecting a POC device or provider
  • Economics of the POC model for pharma
  • Infrastructure needed to make POC work in pharma
  • When in the drug development cycle is the right time to bring in a companion diagnostic?
  • Who should own the test?
  • Who should develop it?
  • Can central labs obviate the need for POC in clinical trials?
  • Which POC tests are ready for market?

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.


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