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FDA Provides Details on Compliance Priorities, New Inspection Protocol Program
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Industry Questions FDA Authority to Collect Quality Metrics
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Managing the Drug Supply Chain: Best Practices
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The New Excipient GMP Standard: A Guide for Drugmakers
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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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Electronic Document Management Systems for Drugmakers
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Electronic Batch Recording and Batch Release for Drugmakers
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Wockhardt Recalls Thousands of Drugs for Third Time Since April
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FDA: Take Lifecycle Approach to Analytical Methods Validation
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EMA Outlines Requirements for Manufacturing Finished Dosage Forms
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New Excipient GMPs in EU Take Effect in March
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