EU "world leader" in biosimilar medicines
The "rigorous scientific approach" adopted by the European Union's biosimilar approval pathway has, according to Greg Perry, the director general of the European Generic medicines Association (EGA), "firmly established the EU as the world leader in biosimilar medicines." Mr Perry was speaking at the opening of the Sixth EGA Symposium on Biosimilar Medicines in London, UK.
In 2007, the group noted that 22% of all the marketing applications received under the European Medicines Agency's (EMEA) centralized procedure were for biosimilar or generic products, 10 each. The EGA forecasts an increase in ex-patent biotechnology drugs coming forward for review in 2008.
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