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 Drafting
a study protocol requires consultation between all the different
participants of the study : promoters, investigators, methodologists. 3Es has a
double expertise, both in medicine and in statistics and is therefore
able to propose an adapted methodology keeping in mind study objectives that
they can help formulate in co-operation with the promoters of the study.
3Es
can also further the drafting of the protocol by proposing to formulate the
questions that compose the CRF, whether it be on paper or on-line and
electronic through Internet.
3Es
can assure the homogeneity between the objectives, the methodology and the CRF
is a major factor of success for clinical trials.
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