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While the marketing of the first biosimilar to be approved in the US market, Zarxio, has been delayed due to a court order, the FDA is providing guidance to manufacturers to help them effectively navigate the process of product development.

While lawmakers, payers, and patient advocates are raising a voice against the sky-rocketing costs of the newer breakthorugh agents in cancer, the drug developers can boast a strong start to the year with big sales figures.

A study published in the journal Health Servcies Research found that veterans enrolled in dual programs, the VA care program and a Medicare Advantage plan, did not perform better or worse than those using the VA alone. This is important considering the duplicate spending associated with dual enrollment.

A one-minute look at managed care news during the week of April 20, 2015, including the how payment reform could hurt emergency care and Americans want the government to do something about high drug prices.

Sandoz's biosimilar will be sold under the trade name Zarxio but the FDA has held off on releasing a naming policy for biosimilars, giving the product a "placeholder nonproprietary name" of "filgrastim-sndz."

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