Monthly Archives: August 2012
Drug Reimbursement and the "New Medicaid"
by Tom Norton
A lot has been written about the “state option” created by the Supreme Court ruling on HCR, and what it means to American medicine. Sorting out an opinion will, to a degree, depend on whom you read and what you believe.
But regardless of where you come out on this issue, there is little [...]
Posted in Guest Blog, Legal, Market Access, R&D, Regulatory, healthcare Tagged Affordable Care Act, generics, government, HCR, healthcare, healthcare reform, Medicaid, Obamacare, public policy 1 Comment
Public Interest in Private Science: New Pathways to Measuring R&D Success
Today’s big product story — the apparent end to a decade-long drought in the drug development pipeline — is the prep stage for tomorrow’s big policy question: are industry R&D priorities in synch with the changing burden of disease?
Bristol-Myers Squibb's Summertime Blues
The sun was shining, savory scents were floating out from the grill, the lemonade was mixed and the table was set. But then dark clouds blew in and settled overhead. Bristol-Myers Squibb’s (BMS) picnic got rained out this summer.
One element of the rain out was forecasted long ago; Plavix, the multibillion dollar [...]
Posted in Advertising, Biotech, Deals, FDA, Legal, Marketing, R&D, Regulatory, Safety, Sales, Strategy, compliance, pricing Tagged Bristol-Meyers Squibb, FDA, Office of Prescription Drug Promotion, OPDP, Regulatory, Untitled Letter Leave a comment

As American as Acid Reflux