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   2010| July-September  | Volume 1 | Issue 3  
    Online since October 20, 2010

 
 
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RESEARCH ETHICS
Readability and comprehensibility of informed consent forms for clinical trials
Anvita Pandiya
July-September 2010, 1(3):98-100
PMID:21814628
  4,276 555 -
REGULATORY
Registration of medical devices
Bobby George
July-September 2010, 1(3):90-93
PMID:21814626
  2,069 352 -
RESEARCH SITES
Conducting feasibilities in clinical trials: An investment to ensure a good study
Viraj Rajadhyaksha
July-September 2010, 1(3):106-109
PMID:21814631
  1,898 523 -
CLINICAL DATA MANAGEMENT
Data management redefined
Nimita Limaye
July-September 2010, 1(3):110-112
PMID:21814632
  1,699 321 -
RESEARCH ETHICS
Survey on perceptions of Indian investigators on research ethics
Sutinder Bindra, Puja Kochhar
July-September 2010, 1(3):94-97
PMID:21814627
  1,604 350 -
EDITORIAL
'Consort 2010: A standard for reporting clinical trials revised anew?
Viraj Suvarna
July-September 2010, 1(3):87-89
PMID:21814625
  1,273 258 -
RESEARCH ETHICS
Patient protection in clinical trials in India: Some concerns
Sandhya Srinivasan
July-September 2010, 1(3):101-103
PMID:21814629
  1,207 320 -
CLINICAL RESEARCH METHODOLOGY
Outcomes research and drug development
Sandeep Duttagupta
July-September 2010, 1(3):104-105
PMID:21814630
  1,022 288 -
LETTER
Insights from FDA Warning Letters

July-September 2010, 1(3):113-113
  788 177 -
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