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pro vyhledávání: '"Sheila R. Shulman"'
Autor:
Sheila R. Shulman, Louis Lasagna
Publikováno v:
Journal of Pharmaceutical Marketing & Management. 12:1-6
Autor:
Sheila R. Shulman, Michael Manocchia
Publikováno v:
PharmacoEconomics. 12:312-326
The Orphan Drug Act has become a staple of food and drug law in the US. The experience with the US programme continues to serve as a useful reference point as interest in orphan drug incentive programmes expands globally. This article first reviews d
Autor:
Sheila R. Shulman, Kenneth I. Kaitin
Publikováno v:
PharmacoEconomics. 9:121-133
The Prescription Drug User Fee Act of 1992 authorises the US Food and Drug Administration (FDA) to collect in excess of $US332 million in user fee revenues over a 5-year period. Not only did Congress determine that the revenues would be dedicated to
Autor:
Sheila R. Shulman
Publikováno v:
PharmacoEconomics. 6:71-79
The influence of the Patented Medicine Prices Review Board in restraining the prices of patented drugs has been established over the past 6 years. Recent legislative and policy changes now in place may result in the Board assuming a more influential,
Autor:
Sheila R. Shulman
Publikováno v:
PharmacoEconomics. 1:21-27
The delivery of health care services in the United States is increasingly influenced by the coverage determinations of third-party payers. This paper reviews 3 specific initiatives recently undertaken by the federal government that relate directly or
Publikováno v:
Drug Information Journal. 26:41-52
To generate descriptive data about the process of therapeutic substitution, a survey was conducted in 10 hospitals in the Boston area. Interviews were conducted with 10 Pharmacy and Therapeutics (P...
Autor:
Sheila R. Shulman
Publikováno v:
Drug Information Journal. 32:363-365
Autor:
Sheila R. Shulman, Drusilla S. Raiford
Publikováno v:
The Journal of Clinical Pharmacology. 30:585-587
On june 22, 1987 regulations issued by the Food and Drug Administration in the United States codified procedures for the treatment use and sale of investigational new drugs outside of the clinical trial setting
Autor:
Sheila R. Shulman
Publikováno v:
PharmacoEconomics. 14
Over the past decade, pharmaceutical benefit management companies (PBMs) have assumed an expanded role as intermediaries in the design and administration of pharmacy programmes. PBMs now provide a range of sophisticated, clinically oriented services