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MHRA Boosts Advisory Capacity After Recent Device Safety Crises
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FDA Warns Ventlab Over Nonconforming Material
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FDA Warns Med-Mizer After Patient Wedges Head in Bed
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AMS Form 483 Notes CAPA, Postmarket Surveillance Slips
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St. Jude Gets Short 483 on Test Method Validation
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Medtronic Handed Form 483 on CAPAs, Inspections
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Baxter 483 Covers CAPA, Risk-Assessment Issues
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OSTP Seeks Devicemakers’ Input on Raw Materials
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FDA Warns Smith & Nephew on Recall Notification, GMP Slips
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Commerce Dept. to Submit Key Conflict Mineral Data Next Month
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FDA 4-Year Plan to Spur Increase in Global Regulatory Partnerships
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Expert Warns of UDI Pitfalls, Advises Early Compliance
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