Oct 1, 2011
By:
Ansis Helmanis
Harvey Bale, Jr., MD, former Director-General, IFPMA
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Oct 1, 2011
By:
Ansis Helmanis
Jane Henney, MD, Former FDA Commissioner
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Dec 1, 2010
By:
Ansis Helmanis
The strict regulatory divide between market authorization and price reimbursement iscrumbling in the US. Is industry prepared to adapt or challenge?
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Mar 1, 2010
By:
Ansis Helmanis
Obligations to fund and support costly studies can extend beyond the period of market exclusivity, giving generics competitors an advantage.
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