PharmaPendium
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
