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STAT+: An insider reveals the real goals of prior authorization

This is the online version of STAT’s weekly email newsletter Health Care Inc. Sign up here.

Well, it appears the Associated Press chose violence with this grammar decision. Over my deadbody, AP. This debate has played out so many times, so do I dare ask you, loyal reader: Is it health care or healthcare? bob.herman@statnews.com.

‘The denial is the outcome’

Archelle Georgiou understands Americans’ frustrations with prior authorization. She helped squash the practice before, at what is now the country’s largest health insurance company.

Continue to STAT+ to read the full story…

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This is the online version of STAT’s weekly email newsletter Health Care Inc. Sign up here.

Well, it appears the Associated Press chose violence with this grammar decision. Over my deadbody, AP. This debate has played out so many times, so do I dare ask you, loyal reader: Is it health care or healthcare? bob.herman@statnews.com.

‘The denial is the outcome’

Archelle Georgiou understands Americans’ frustrations with prior authorization. She helped squash the practice before, at what is now the country’s largest health insurance company.

Continue to STAT+ to read the full story…

Read More

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EnGene’s shares crash on updated pivotal bladder cancer data

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EnGene’s latest Phase 2 results on an experimental treatment for certain bladder cancer patients alarmed investors and raised concerns around the therapy’s future prospects.

The Canadian biotech’s shares {$ENGN} fell 80% Thursday morning after reporting …

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Angelini to buy Catalyst in $4B play for rare neuro drugs

The acquisition hands the Italian pharma a group of medicines approved to treat various CNS disorders and gives it wider market access in the U.S.

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The acquisition hands the Italian pharma a group of medicines approved to treat various CNS disorders and gives it wider market access in the U.S.

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FDA reverses course on Atara, Pierre Fabre’s twice-rejected cell therapy after Prasad’s exit

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The FDA turned away Ebvallo in January, taking issue with the design of the registrational trial. In a recent meeting, however, the agency agreed that the study could in fact support the cell therapy’s approval. The news comes a week after the departure of controversial biologics Director Vinay Prasad.

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