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 The
quality level of a clinical trial determines the admissibility of its results.
Study
management for phase I, II, or phase III clinical trials for the pharmaceutical
industry, public institutions, or federations represents an activity in
constant progression at 3Es.
Our
partners continually renew their confidence based on the successful results of
our quality services. 3Es drafts the protocols, the CRFs and all
administrative and legal documentation necessary for your study set-up. Through
our expertise and in-house tools, 3Es integrates all of the different steps for
clinical data management : from randomisation to different stages of data
management and reporting. Statistical analysis combined with medical
interpretation as well as scientific valorisation through international
publications are part of the services 3Es can provide.
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