Batch variability in pharmaceutical manufacturing can skew bioequivalence results, leading to incorrect approvals or rejections of generic drugs. Learn how regulators are updating standards to account for real-world manufacturing differences.
Continue ReadingHospital formularies carefully select generic drugs based on clinical safety, cost, and supply reliability-not just price. Learn how P&T committees evaluate generics, navigate rebates, and manage shortages to ensure patient care isn't compromised.
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