ASBM Letter to Idaho Board of Pharmacy

August 6, 2014

The Idaho Board of Pharmacy held a hearing on August 5th and 6th regarding proposed regulations for the treatment of biosimilars in their state.  View ASBM letter here.

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Senate HELP Committee authors letter to HHS Secretary on biosimilars issues

August 1, 2014

View letter here.

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Senate HELP Committee authors letter to HHS Secretary on biosimilars issues

August 1, 2014

View letter here.

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Senator Hagan writes HHS to issue guidance on naming

July 30, 2014

View letter here.

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Senator Hagan writes HHS to issue guidance on naming

July 30, 2014

View letter here.

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ASBM member RetireSafe conducts senior survey on knowledge and safety issues concerning biosimilars

July 18, 2014

A new RetireSafe survey, published July 15th, finds seniors largely are unaware of “biosimilar” drugs and overwhelmingly support strong patient safeguards for biosimilar development and FDA approval. In the survey, senior respondents supported robust clinical trials, unique names for biosimilar drugs, as well as physician and patient notification of biosimilar substitution. To view the RetireSafe […]

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Pennsylvania has a chance to update its law to allow for biosimilar medicine substitutions – Pittsburgh Post Gazette

July 9, 2014

See article here.

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Pennsylvania has a chance to update its law to allow for biosimilar medicine substitutions – Pittsburgh Post Gazette

July 9, 2014

See article here.

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EU Commission publishes “What you need to know about biosimilar medicinal products”

July 9, 2014

Translations of the European Commission’s Consensus Information Document on biosimilars is now available in French, German, Italian and Spanish. The documents were created to foster stakeholders’ understanding of biosimilars in Member States and is a result of a cooperation of all relevant European stakeholders.  The papers can be found on the European Commission’s website. Also to learn more […]

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EU Approves First Biosimilar Insulin

July 1, 2014

On June 27, the European Medicines Agency’s (EMA’s) Committee for Medicinal Products for Human Use (CHMP) announced granting of preliminary marketing approval for the European Union’s first biosimilar insulin glargine product. Called Abasria (LY2963016), the investigational basal (long-acting) insulin is intended for the treatment of type 1 and type 2 diabetes. Abasria, like its reference product, the […]

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