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Australia Clarifies Postmarket Reviews of Subsidized Drugs
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Drug Approval Backlog Nears 19,000 in China
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Japan Clarifies Premarket Review Routes for Combination Products
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Ebola Vaccine Developers Protected From Liability Under U.S. Law
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New Zealand Moves Forward On Updating Recall Procedures
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EFPIA Proposes Process for Early Resolution of Patent Disputes
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Consolidation of Drug Import Oversight Aimed at Harmonizing U.S. Port Policies
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U.S. FDA May Recognize Firms That Go Extra Yard in GMP Compliance
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India’s Drug Pricing Authority Sets Prices on 52 More Products
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India Releases Draft Standards On Trial Ethics, Accreditation
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EU States Suspend Marketing Nods For Generics Vetted by GVK
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Biosimilars Makers Press for Dose API as Reference Comparator
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