The Post-Exclusivity Event Horizon: Strategic Forecasting of Generic and Biosimilar Entry
Pharmaceutical life cycle management begins earlier and ends later to maximize stakeholder value in all phases of drug development.
Pharmaceutical life cycle management begins earlier and ends later to maximize stakeholder value in all phases of drug development.
For readers following the the Biologic Patent Transparency Act, DrugPatentWatch has recently been cited in an article describing the act as
DrugPatentWatch in the news: The Biologic Patent Transparency Act. Read Post »
1. What This Article Covers and Why It Matters Now The baseline 20-year patent term for a small molecule drug
Healthcare systems including hospitals are taking care-related and business-related steps to cope with rapidly increasing drug prices.
Information contained in expired drug patents can be invaluable to researchers developing new products, but caution is required to avoid legal problems.
A comprehensive analysis for pharma IP teams, portfolio managers, payer strategy leads, and institutional investors examining the structural economics, IP
The global generic drugs market was valued at $468.08 billion in 2025 and is projected to reach $728.64 billion by
An evidence-based analysis of FDA-approved oncology drug economics, patent strategy, and what the numbers actually mean for payers, investors, and
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Recent successful drug launches indicate a trend toward more specialized, high-priced drugs that treat less-common medical conditions.
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