Gianfranco De Feo, Giacomo Chiabrando, Nunzia Cannovo, Antonio Galluccio, Carlo Tomino
Abstract
The high variability of "centre-specific" documentation required by Independent Ethics Committee (IEC) plays a role in the time required for activation of participating centres of multicentre clinical trials. This study (a) provides a picture of the different activities, structural requirements and resources dedicated to the operation of the local IEC in Italy; (b) defines a detailed list of "centre-specific" documents considered as essential by the IEC for issuing its opinion and (c) suggests a "single document" to reduce the variability of the "centre-specific" documents required by the IEC.
This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 26 November 2012.
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#15,256,901
of 22,687,320 outputs
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#129,945
of 193,653 outputs
Outputs of similar age
#115,468
of 183,506 outputs
Outputs of similar age from PLOS ONE
#2,991
of 4,904 outputs
Altmetric has tracked 22,687,320 research outputs across all sources so far. This one is in the 22nd percentile – i.e., 22% of other outputs scored the same or lower than it.
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