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PharmaPendium provides manually extracted and full-text searchable FDA and EMA approval packages to help:

• predict success of drug candidates

• reduce animal testing

• anticipate post-market safety risks

• optimizing clinical trial design

• check for DDIs

• reduce risks of off-target related AEs

The Tox Navigator (new!) provides quick analysis of drug candidates’ toxicity profile:

• facilitate ADR investigations across different species and converts animal doses to human equivalent doses (HED)

• provide early identification of safety risks, translational toxicology, and regulatory compliance

The world’s largest solution for biomedical literature for safety evaluation and prioritization.

• Track drug-disease relations

• Recognized by regulatory bodies as a source for discovering adverse events