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Social media enthusiast at the intersection of IT and Health care. Employee of The Drug Information Association: The Global Forum for Therapeutic Innovation & Regulatory Science - A Neutral, Nonprofit Association

Sunday, April 7, 2013

Nonclinical and Translational /Early Phase Clinical Development Track at DIA's 49th Annual Meeting

 
  • How can we optimize the transition from Preclinical to Clinical Research?
  • How can we design a strategy for efficient, rapid and inexpensive assessment of drug-related QT effects?

  • What is the Impact of Subject Dual Enrollment on Study Data Validity?

  • What are the opportunities for drug-induced vacsulitis biomarkers and translational medicine research areas.

  • What are the benefits of PET imaging in preclinical and clinical therapeutic drug development?

  • What is the impact of Pharmacometrics in Preclinical to Early Phase Clinical Development?
  • When are human abuse liability studies indicated by FDA?  

  • What is the impact of regional cooperation on drug development innovation in China and Latin America?
Posted by Unknown at 11:22 AM
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Labels: #DIA2013, biomarkers, China, clinical development, Clinical Research, clinical therapeutic drug development, DIA2013, FDA, Latin America, nonclinical, Track 4, translational development, translational medicine

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