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Institute Proposes Online Registry to Increase Drugs Transparency
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USTR Review of India’s IP Rights to Focus Largely on Pharma
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Pharma Exclusivity Could Be Sticking Point on Trans-Pacific Partnership Pact
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EU Medicines Policy Remains Under Health Directorate Oversight
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ADR Database Now Covers Broader Swath of Suspected Drug Reactions
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Ebola Treatments Put on Fast Track for Approval at EMA, U.S. FDA
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Australia Endorses EU Guideline on Vaccine Pharmacovigilance
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Aussie Guidance Details Nonclinical Requirements for Drug Registration
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Centralized Review of Some Nationally Authorized APIs Now Required in EU
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NICE Board Opts to Keep Current Evaluations Guide for Time Being
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MHRA Explores Using Social Media to Report Adverse Drug Events
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India Withdraws Internal Guideline for Setting Drug Price Controls
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