ComplianceOnline, Online Event
2012-11-08
Why Should You Attend: This 90-minute session will review the new and expected regulations/ technologies and discuss their effects on the use of pharmacogenomics in industry. We will explain what the policies are, predict coming regulations and discuss how industry will be affected. We will explore the personalized medicine landscape in US, EU and globally.
All functional groups who have drugs responsibility or need to understand the basics of pharmacogenomics and personalized medicine will benefit by participating in this webinar. Areas Covered in the Seminar: - Overview of Pharmacogenomics, applications and challenges.
- From Pharmacogenomics to Personalized Medicine.
- PharmacoGenomics Data, genetic tests and Biomarkers.
- FDA(US) guidances and federal initiatives(NIH, CDC, CMS).
- EMEA (EU), Health Canada guidances and global landscape.
- Clinical Genomics data standards (EHR, HL7, ISO, Healthcare).
- Drug/Healthcare industry and pharmacogenomics.
- Pharmacogenomics and Ethical issues.
- Future of Genomics Medicine.
Event Details: Date: November 08, 2012 Time: 10:00 AM-11:30 AM PST Cost: $299 per attendee per computer terminal Registration: SIgn-Up on-line now. Add to your shopping cart. |
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