π Dataset Summary
The Pharmaceutical Approvals & Regulatory Timeline Data captures 500 drug approval records drawn from the four major regulatory jurisdictions: China (NMPA), United States (FDA), European Union (EMA), and Japan (PMDA), with approximately 100 records per region. It enables comparative regulatory analysis and temporal modeling of the global pharmaceutical approval landscape.
π Key Features
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Four-Jurisdiction Coverage: Balanced representation across China, US, EU, and Japan⦠See the full description on the dataset page:
https://huggingface.co/datasets/PatSnap/drug-approvals.