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Robert Califf Fends Off Senators’ Questions on Generics, Biosimilars During Hearing
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Panelists Say Biosimilars Market Needs Regulatory and Patent Changes to Grow
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Brazil’s Anvisa Suspends Deadline for New Drug Tracking Program
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Poorest Nations Exempt From WTO Patent Rules for Next 17 Years Under Agreement
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Indian Government Pitches New Plan to Boost Drug Regulation System
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EU Ombudsman Clears EMA Over Decision to Redact Clinical Trial Reports
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Japan’s Sakigake Approval Pathway Aims to Cut Drug Lag, Expert Says
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EFPIA Lays Out Biosimilars Competition Plan to Sustain Industry With Incentives
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EMA Updates Drugmakers on Plans for Reforming Pharmacovigilance
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Text of Trade Deal Shows That Eight Years of Market Exclusivity Is Not Guaranteed
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FTC OKs Mylan-Perrigo Deal, Demands Sale of Seven Generics
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Senate Passes Bill to Extend Marketing Exclusivity Period
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