Dropped Claims Don’t Lie
How Abandoned ANDA Litigation Patents Predict Weaker Enforcement The Most Underrated Signal in Generic Drug Intelligence When a brand pharmaceutical […]
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Pharmaceutical Supply Chain Resilience: Lessons from the Pandemic
The pharmaceutical supply chain is a complex, multi-tiered network that historically has been optimized for efficiency and cost reduction above
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The 1,825-day head start: How to stop a generic without a patent
Investors and executives often treat the expiration of a composition-of-matter patent as the singular moment of truth in a drug’s
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Orange Book vs. Purple Book: Strategic Differences for Small Molecule vs. Biologics Competition
The strategic landscape of the modern pharmaceutical and biotechnology industries is bifurcated by two distinct regulatory and legal architectures that
Decoding the FDA Orange Book’s Therapeutic Equivalence (TE) Codes for Generic Drug Substitution Strategy
The regulatory framework of the United States pharmaceutical industry is governed by a complex interplay of scientific evaluation, legislative compromise,
The Billion-Dollar Blockade: How to Dismantle Drug Patent Thickets and Reclaim the Market
The pharmaceutical landscape in the United States is currently defined by a paradox: a system designed to foster innovation has
The 180-Day Prize: Using Orange Book Patent Data to Secure Early Market Control
Economic success in the generic pharmaceutical industry depends on timing. Between 2026 and 2030, blockbuster drugs representing an estimated $236
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The Math of Monopoly: Why a 20-Year Drug Patent Lasts Only 12 Years
The 20-year patent term is a nominal legal baseline that rarely reflects the commercial reality of a pharmaceutical product. While
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Know Before the Cliff: How to Forecast Drug Patent Expiry
The Billion-Dollar Blind Spot in Pharmaceutical Strategy Every year, pharmaceutical executives sit in board meetings with revenue projections that quietly
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