EMA Posts Biosimilars Q&A to Help Clarify Presubmission Meetings

April 30, 2012
The European Medicines Agency (EMA) has published question-and-answer guidance on marketing applications for biosimilars, providing advice on a number of pre-submission issues, such as requesting an accelerated assessment, and giving detailed answers about review timing. The guidance collects various regulatory and procedural questions already published on the EMA’s website and should be read in conjunction with the agency’s scientific guidelines on biosimilars, the EMA said April 11.
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