The standard Paragraph IV playbook was written for atorvastatin and metformin, not for drugs prescribed to 800 patients nationwide. When […]

The pharmaceutical vendor ecosystem — CROs, CDMOs, biomarker platform providers, data analytics firms, and laboratory services companies — has spent

The FDA’s Purple Book is supposed to be the authoritative public registry for biologic drug patents in the United States.

How combination patent architecture protects pharmaceutical revenue after composition-of-matter expiry — and what the post-Teva v. Amneal landscape means for

When a small-molecule drug loses its composition-of-matter patent, the conventional story is that the clock runs out and generic manufacturers

Two protection systems govern pharmaceutical market exclusivity in the United States. One is a private intellectual property right, contested in

Most pharmaceutical companies treat patent disclosures as a legal obligation. The better ones treat them as a revenue forecast. The

The short answer is: yes, you can use PAT-INFORMED to find drug patent information, including grant dates and expiry dates

For most of the 20th century, pharmaceutical intellectual property was a single-act play. You discovered a molecule, filed a composition-of-matter