FOXYMED, in close collaboration with the client, can liaise with the author and take care of the publication from conception to submission to the target journal.
FOXYMED participates in the writing of regulatory documents intended for Health Authorities: New Drug Application dossier, safety & efficacy documents, clinical and research documents…
FOXYMED accomplishes accompaniments for clinical trials: protocols, Clinical Study Report (CSR), data analysis, presentations for experts meeting, liaison with statistician for later or post-hoc analysis…
Literature review can be provided by FOXYMED: medline searches, digests, preparation of syntheses, critical appraisals, clinical & research documents…
FOXYMED can help to the preparation of an expert meeting by organizing logistics, preparing slides and documents, animate and moderate the meeting and eventually preparing reports.
Consulting & Management
FOXYMED intervenes in the following areas: constitution of scientific advisory boards, recommendation for publication strategy, development of a publication plan, participation in project teams…
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