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   2010| October-December  | Volume 1 | Issue 4  
    Online since October 20, 2010

 
 
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QUALITY
Good clinical practice regulatory inspections: Lessons for Indian investigator sites
R Marwah, K Van de Voorde, J Parchman
October-December 2010, 1(4):151-155
DOI:10.4103/2229-3485.71776  PMID:21350732
  10,528 647 2
RESEARCH ETHICS
Informed consent: Are we doing enough?
Pranati
October-December 2010, 1(4):124-127
DOI:10.4103/2229-3485.71769  PMID:21350726
  2,725 829 1
REGULATORY
Regulatory requirements for marketing fixed dose combinations
BG Jayasheel
October-December 2010, 1(4):120-123
DOI:10.4103/2229-3485.71768  PMID:21350725
  2,770 691 1
CLINICAL DATA MANAGEMENT
Ensuring on-time quality data management deliverables from global clinical data management teams
Zia Haque
October-December 2010, 1(4):143-145
DOI:10.4103/2229-3485.71774  PMID:21350730
  2,831 436 -
DRUG DEVELOPMENT
Personalized medicine: Striding from genes to medicines
Sunita R Nair
October-December 2010, 1(4):146-150
DOI:10.4103/2229-3485.71775  PMID:21350731
  2,407 628 6
TRAINING
Training needs of clinical research associates
Samyuktha Ajay, Arun Bhatt
October-December 2010, 1(4):134-138
DOI:10.4103/2229-3485.71771  PMID:21350728
  2,249 715 1
CLINICAL RESEARCH METHODOLOGY
Non interventional drug studies in oncology: Why we need them?
Divya Mishra, Jesal Vora
October-December 2010, 1(4):128-133
DOI:10.4103/2229-3485.71770  PMID:21350727
  2,403 449 3
EDITORIAL
Training for clinical research professionals: Focusing on effectiveness and utility
Viraj Rajadhyaksha
October-December 2010, 1(4):117-119
DOI:10.4103/2229-3485.71767  PMID:21350724
  1,499 510 1
TRAINING
Trials and tribulations of clinical research teaching and training
Ravindra B Ghooi
October-December 2010, 1(4):139-142
DOI:10.4103/2229-3485.71773  PMID:21350729
  1,556 308 -
FACTS AND FIGURES
Indian clinical research industry
Melanie Fernandes, Arun Bhatt
October-December 2010, 1(4):156-156
PMID:21350733
  904 351 -
ANNOUNCEMENT
Announcement

October-December 2010, 1(4):157-158
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