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Cardiovascular Safety in Drug Development: QT, Arrhythmias, Thrombosis, and Bleeding

 
  January 26, 2010  
     
 
DIA, Arlington, VA 22204
Apr 11 2010 8:00AM - Apr 13 2010 5:00PM


Date(s) And Time(s):
Apr 11 2010 8:00AM - Apr 13 2010 5:00PM

Location:
Sheraton National Hotel Arlington
900 South Orme Street
Arlington, VA 22204 

Interest Area(s):
Clinical Safety/Pharmacovigilance, Clinical Research, Document Management/ eSubmissions, Nonclinical, Quality Assurance/Quality Control, Regulatory Affairs, Research & Development

Overview:

Abstract Submission Guidelines

Please submit all abstracts via email to Rachel Minnick, Program Developer Rachel.Minnick@diahome.org

All abstracts must be received by February 13, 2010

Authors of selected abstracts will be notified by March 13, 2010

 Suggested Abstract Topics

(The strongest abstracts have been those with a clear hypothesis and supporting data with a strong scientific design)

Drug Development and CV safety

·         Drug-induced increases in CV events

·         Myocardial toxicity

·         Pharmacogenomics and drug-induced CV injury

·         How can we practically assess the negative inotropic potential of new drugs?

·         Anticoagulant safety—how to measure it?

Evolving Science of QT/Arrhythmia Assessment


 

Target Audience:

Who Should Attend

·         Academic scientists

·         Industry management

·         Clinical project physicians

·         Quality assurance directors

·         Preclinical/discovery scientists

·         ECG safety data managers

·         ECG lab and equipment vendors

·         Regulatory specialists

 
 
Organized by: Rachel Minnick
Invited Speakers: call contact
 
Deadline for Abstracts: call contact
 
Registration:
 

For further information, contact Rachel Minnick, Program Developer Phone +1.215.442.6131 | Fax +1.215.293.5904 Rachel.Minnick@diahome.org

 

E-mail: Rachel.Minnick@diahome.org
 
   
 
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