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FDA Updates Refuse-to-Receive Rules for ANDA Submissions
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FDA Developing Bioinformatic Approach to Evaluating Generics
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New Rules on Plain Language Labeling Take Effect in Canada
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FDA Advises Sponsor Investigators on INDs
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Experts: Data from Women Key to Successful Trials
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FDA Invites Feedback on LOINC Coding for Clinical Trial Lab Results
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EMA Clarifies Clinical Requirements for Fixed-Dose Combinations
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CXL-USA Warned Over Unapproved Clinical Trial
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Pharma Increasing Reporting of Clinical Trial Results: Study
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21st Century Cures Act Sails Through House Committee
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FDA Overhaul Bill Clears U.S. House Panel, Heads to Floor Vote
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Australia Looking to Reform Orphan Drug Regulations
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