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 We propose
a complete study management and set-up for data collection adapted to
the :
- Study type (observation, transverse study, cohort study…)
- Implication of participants (Medical and non -medical)
- Future use of study results
This set-up
also includes provisioning of study documents (protocol, observation log,
synopsis and information to the medical Investigator) as well as notification
of the Data base to the CNIL by the study promoter.
Particular
studies imply legal notification to the CCPPRB, to the CNOM and the AFSSAPS.
Our Quality specialist will help you in these different steps.
Interpretation
of data, after statistical processing, depends on the quality of the
collection process and the transformation of clinical information into
analysable data.
3Es offers
the possibility, for the duration of the study, to use a complete computerised
infrastructure to realise data collection by Internet. Using INES,
our user friendly in-house software is so simple, Investigators do not
need any formal training. Assistance by e-mail or phone is sufficient
to pass the different steps from the connection to the collection of data
via Internet.
Use of
Internet and access to the software in French or in English allows international
study management without any additional complications.
We also
propose to organise half-day meetings for Investigators concerning awareness
of study objectives and the importance of quality
data.
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