Table of Contents

2016| July-September  | Volume 7 | Issue 3  

EDITORIAL
	How informed are our subjects?	p. 109
	Ravindra B Ghooi
	[ABSTRACT]  [HTML Full text]  [PDF]
REVIEW ARTICLES
	Reporting of adverse events for marketed drugs: Need for strengthening safety database	p. 111
	Aditi Anand Apte
	[ABSTRACT]  [HTML Full text]  [PDF]
	Emerging role of bioinformatics tools and software in evolution of clinical research	p. 115
	Supreet Kaur Gill, Ajay Francis Christopher, Vikas Gupta, Parveen Bansal
	[ABSTRACT]  [HTML Full text]  [PDF]
ORIGINAL ARTICLES
	Comparison of good clinical practice compliance and readability ease of the informed consents between observational and interventional clinical studies in the Emirates	p. 123
	Satish Chandrasekhar Nair, Halah Ibrahim, Omar Sherif Askar
	[ABSTRACT]  [HTML Full text]  [PDF]
	Assessment of adherence to the statistical components of consolidated standards of reporting trials statement for quality of reports on randomized controlled trials from five pharmacology journals	p. 128
	Sachin Satpute, Manthan Mehta, Sandeep Bhete, Dnyneshwar Kurle
	[ABSTRACT]  [HTML Full text]  [PDF]
	Assessment and classification of protocol deviations	p. 132
	Ravindra Bhaskar Ghooi, Neelambari Bhosale, Reena Wadhwani, Pathik Divate, Uma Divate
	[ABSTRACT]  [HTML Full text]  [PDF]
	Challenges in recruitment and retention of clinical trial subjects	p. 137
	Rashmi Ashish Kadam, Sanghratna Umakant Borde, Sapna Amol Madas, Sundeep Santosh Salvi, Sneha Saurabh Limaye
	[ABSTRACT]  [HTML Full text]  [PDF]
STATISTICS
	Common pitfalls in statistical analysis: Intention-to-treat versus per-protocol analysis	p. 144
	Priya Ranganathan, CS Pramesh, Rakesh Aggarwal
	[ABSTRACT]  [HTML Full text]  [PDF]
LETTER TO EDITOR
	Single-versus double-masking in glaucoma clinical trials	p. 147
	DL DeMill, Barbara M Wirostko, Lindsay A Nelson, Jeanette A Stewart, William C Stewart
	[ABSTRACT]  [HTML Full text]  [PDF]