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U.S., EU Expand Collaboration on Drug Development, Inspections
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U.S. FDA Sets Dissolution Specs for Immediate-Release Drugs
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ICH Updates Guidance on Two Pharmaceutical Solvents
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Canada to Require GMP Compliance Evidence for All Foreign Facilities
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EU Clarifies Manufacturing Requirements for FDFs
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EMA Revising Draft Guidelines on Fast-Track Approval Paths
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Japan Outpaces Europe, U.S. in 2014 Drug Approvals
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China Reports Slight Uptick in ADR Cases Last Year
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Drugmakers to Focus on 10 Data Points in U.S. Quality Metrics Thrust
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CFDA to Begin Conducting Surprise Inspections
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China Requiring Sponsors to Show GCP Compliance
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European Commission Bans Scores Of Drugs Due to Flawed Studies
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