Amgen welcomes European Commission report on EU biosimilars uptake
MISSISSAUGA, ON, April 30, 2013 /CNW/ - Amgen, a biotechnology company
developing both innovative biologic and biosimilar medicines, welcomes a new
report from the European Commission detailing Europe's strong regulatory and
commercial foundation for biosimilars in the healthcare marketplace. The
report shows that biosimilars are helping improve competition and thus may be
increasing access to biologic medicines for patients.
The science-led regulatory framework in the European Union (EU) has
established confidence in biosimilars which has allowed for these therapeutic
alternatives to successfully enter into clinical practice. As governments,
industry and the healthcare sector work together to improve health outcomes,
the report reaffirms that protecting patient safety is the cornerstone of the
EU's regulatory framework for biosimilar medicines.
Amgen, a core stakeholder in the consultation process for this report,
welcomes the opportunity this consensus document provides for ongoing balanced
and informed discussions on the European biosimilars experience. This report
is designed to help national governments, health care professionals and
patients make informed choices on the role current and future biosimilar
medicines may have in achieving optimal healthcare outcomes.
For more information or to set up an interview, please contact:
Natasha Bond Amgen Canada Tel: 905-285-3007 Email:email@example.com
SOURCE: Amgen Canada
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CO: Amgen Canada
-0- Apr/30/2013 12:30 GMT
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