Perspectives in Clinical Research
Table of Contents

2010| October-December | Volume 1 | Issue 4
Please wait, loading Google Map...
EDITORIAL | ||
Training for clinical research professionals: Focusing on effectiveness and utility | p. 117 | |
Viraj Rajadhyaksha | ||
[ABSTRACT] [HTML Full text] [PDF] | ||
REGULATORY | ![]() |
|
Regulatory requirements for marketing fixed dose combinations | p. 120 | |
BG Jayasheel | ||
[ABSTRACT] [HTML Full text] [PDF] | ||
RESEARCH ETHICS | ![]() |
|
Informed consent: Are we doing enough? | p. 124 | |
Pranati | ||
[ABSTRACT] [HTML Full text] [PDF] | ||
CLINICAL RESEARCH METHODOLOGY | ![]() |
|
Non interventional drug studies in oncology: Why we need them? | p. 128 | |
Divya Mishra, Jesal Vora | ||
[ABSTRACT] [HTML Full text] [PDF] | ||
TRAINING | ![]() |
|
![]() |
Training needs of clinical research associates | p. 134 |
Samyuktha Ajay, Arun Bhatt | ||
[ABSTRACT] [HTML Full text] [PDF] | ||
Trials and tribulations of clinical research teaching and training | p. 139 | |
Ravindra B Ghooi | ||
[ABSTRACT] [HTML Full text] [PDF] | ||
CLINICAL DATA MANAGEMENT | ![]() |
|
Ensuring on-time quality data management deliverables from global clinical data management teams | p. 143 | |
Zia Haque | ||
[ABSTRACT] [HTML Full text] [PDF] | ||
DRUG DEVELOPMENT | ![]() |
|
![]() |
Personalized medicine: Striding from genes to medicines | p. 146 |
Sunita R Nair | ||
[ABSTRACT] [HTML Full text] [PDF] | ||
QUALITY | ![]() |
|
Good clinical practice regulatory inspections: Lessons for Indian investigator sites | p. 151 | |
R Marwah, K Van de Voorde, J Parchman | ||
[ABSTRACT] [HTML Full text] [PDF] | ||
FACTS AND FIGURES | ![]() |
|
Indian clinical research industry | p. 156 | |
Melanie Fernandes, Arun Bhatt | ||
[ABSTRACT] [HTML Full text] [PDF] | ||
ANNOUNCEMENT | ![]() |
|
Announcement | p. 157 | |
[ABSTRACT] Full Text not available [PDF] | ||