«
The clear results of the present study open a wide door to a therapeutic advance.
Not exact matches
A second letter, from David Hawkes, a viro logist at the University
of Melbourne in Australia, and two colleagues argues that the paper «lacks a
clear methodology, adequate controls to control for bias, descriptions
of results consistent with the data
presented, or enough information for this
study to be reproduced.»
The documentation ranges across the whole spectrum
of drug development: Investigators» brochures provide information on all that is currently known about the medicine and so need periodic updating; accurate and concise protocols are required to ensure that trials are performed effectively; clinical trial reports (generally from phase II and III
studies)
present the information gathered from the trials; higher level documents provide summaries
of efficacy and safety data from clinical trial programmes; expert reports provide critical interpretation
of the
results; and response documents clarify any points that are not
clear to the regulatory agencies or provide additional analyses or supporting data for any items
of concern.
Furthermore, Custom Case -
study assignment writing need conceptualization
of all the evident facts, detailed analysis
of the facts, discussion and interpretation which
results in
clearing up the
present conditions or situations.