EMA plans to revise current guidance on quality issues for biosimilars

This article was originally published in SRA

02 Mar 2011
News

Vibha Sharma @ScripRegVibha vibha.sharma@informa.com

Executive Summary

The European Medicines Agency is planning to revise its guideline dealing with quality requirements for similar biological medicinal products containing biotechnology-derived proteins as active substance^1.

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EMA plans to revise current guidance on quality issues for biosimilars

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