Are you researching drug labels, the regulatory intelligence landscape, scientific literature and clinical trials with multiple open browser tabs? Are you finding and comparing multiple sources, piecing together an answer, and manually tracking everything on spreadsheets? There's a better way.
Trust Dr.Evidence, the first and most experienced innovator to bring life sciences intelligence into one location to streamline your work. We bring pharmaceutical labeling, regulatory, commercial, safety, clinical trials and scientific literature into a single, unified platform. Transform how your team works— from regulatory submission through commercialization— with a platform that accelerates decision-making, de-risks strategy, and delivers results you can trust.
time to insight, conducting complex regulatory analysis in hours instead of weeks.
labels, drug applications, clinical trials and scientific literature into a unified workflow.
fragmented evidence from multiple sources into a clear decision pathway.
time-intensive and manual tasks so you can focus on strategic work at the top of your capabilities.
securely in-platform with colleagues across your organization.
your analysis with human-in-command fit-for-purpose AI summaries and insights.
Created the pharma landscape intelligence space, with continuous innovation
20+ years of domain experience
25+ proprietary AI models with zero IP leakage
Complimentary white-glove search optimization and ongoing support
728,000+ labels from 11 major health authorities
Centralizes U.S. drug labels from Drugs@FDA, DailyMed, Orange Book, Purple Book, and more
Generate side-by-side comparisons instantly
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1.1 million clinical trials
70 million scientific literature citations
400,000 congresses
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31 million patents and 500,000 NIH grants
2.1 million articles from healthcare RSS feeds
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140,000 FDA and EMA approval packages
4,000 FDA and EMA Guidance documents
49,000 Orange and Putple Book data points
Drug labels, regulatory approval packages and guidance published by health authorities across the globe, clinical trials from WHO ICTRP, and scientific literature from PubMed and a range of other reputable sources.
with AI-powered workflows built specifically for biopharma
so your experts can focus on high-value strategy
with contemporary, evidence-driven market insights
by eliminating manual work and automating monitoring
Whether you’re tracking label changes, preparing submissions, or analyzing competitive prior precedent, Dr.Evidence helps you move faster with confidence. Reach out, and our team will follow up to understand your needs and show you what’s possible.
Find quick solutions to common questions about our platform and services.