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Perspectives in Clinical Research

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2010| October-December  | Volume 1 | Issue 4  

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EDITORIAL  
Training for clinical research professionals: Focusing on effectiveness and utility p. 117
Viraj Rajadhyaksha
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REGULATORY Top
Regulatory requirements for marketing fixed dose combinations p. 120
BG Jayasheel
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RESEARCH ETHICS Top
Informed consent: Are we doing enough? p. 124
Pranati
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CLINICAL RESEARCH METHODOLOGY Top
Non interventional drug studies in oncology: Why we need them? p. 128
Divya Mishra, Jesal Vora
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TRAINING Top
Training needs of clinical research associates p. 134
Samyuktha Ajay, Arun Bhatt
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Trials and tribulations of clinical research teaching and training p. 139
Ravindra B Ghooi
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CLINICAL DATA MANAGEMENT Top
Ensuring on-time quality data management deliverables from global clinical data management teams p. 143
Zia Haque
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DRUG DEVELOPMENT Top
Personalized medicine: Striding from genes to medicines p. 146
Sunita R Nair
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QUALITY Top
Good clinical practice regulatory inspections: Lessons for Indian investigator sites p. 151
R Marwah, K Van de Voorde, J Parchman
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FACTS AND FIGURES Top
Indian clinical research industry p. 156
Melanie Fernandes, Arun Bhatt
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ANNOUNCEMENT Top
Announcement p. 157
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