Incorporating Pharmacogenomics in Clinical Studies

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Incorporating Pharmacogenomics in Clinical Studies

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September 25 - September 26 2006 | Hyatt Regency - Inner Harbor | Baltimore, MD

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Who Should Attend

Primary market:
Scientists and clinical operations professionals working at pharmaceutical, central labs and specialized diagnostic labs

TITLES:

Clinical Research
Clinical Trial Design
Medical Director
Biomarker Development
Clinical pharmacologists
Human Geneticists
Molecular biologists
Pharmacogenomics
Chief Scientific Officers
Scientific Director
Medical Affairs

Clinical Sciences
Clinical Research Scientists
Clinical Operations
Medical Services
Assays Developers
Project Managers
Regulatory Affairs
Cardiologists
Oncologists
Data Management

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The Institute for International Research works with many accreditation boards such as NASBA, ACPE, CLE, and the Thomas Beam Institute, to give you the opportunity to receive continuing education credits. To learn more about accreditations, contact La Shawn Jackson, the Continuing Education Coordinator, at ljackson@iirusa.com.

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Incorporating Pharmacogenomics in Clinical Studies

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Who Should Attend

Who Should Attend

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