The European Medicines Agency (EMA) has released revised guidance to answer questions about the process of seeking scientific advice from the agency, including an overview of the scientific advice process and how to prepare a request for scientific advice.
EMA's Guidance for Companies Requesting Scientific Advice, the third revision of which was released on 15 May 2012, covers pre-submission meetings where companies request guidance from EMA staff on scientific issues before submitting their application for approval.
These meetings typically occur 1-2 months before the submission of a dossier, and cover a wide range of topics. EMA's 15 May revision to the guidance addresses 16 topics of interest to sponsors, and answers some common questions.
EMA's guidance explains:
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