Puraite – Real Time Medical Evidence
Puraite is transforming the systematic review process in medical research with AI-powered screening and data extraction methods.
Our Mission
Revolutionizing Medical Research
Our Mission Statement:
Puraite's mission is to revolutionize medical research by embracing these core values:
Accelerating Time-to-Insight
We deliver rapid, evidence-backed answers to your critical medical research questions.
Advanced AI Technology
Harnessing cutting-edge AI techniques that push the boundaries of innovation.
Full Transparency
Our models are fully transparent, ensuring human traceability every step of the way.
EXPLORE BY INDUSTRIES
Transform Your Pharmaceutical Workflow
Regulatory Affairs Teams
Full systematic reviews and meta-analyses prepared for EMA/FDA submissions. These synthesize clinical trial evidence into structured, PRISMA-compliant packages used to demonstrate benefit-risk profiles for marketing authorization.
Market Access & HEOR Teams
Evidence synthesis for HTA dossiers (e.g., NICE, G-BA, HAS). Reviews compare effectiveness and cost-effectiveness across multiple trials, supporting pricing, reimbursement, and early access negotiations.
Regulatory Affairs Managers
Systematic reviews for MDR/IVDR-compliant Clinical Evaluation Reports (CERs) and Performance Evaluation Reports (PERs). They consolidate device-specific evidence to demonstrate safety and performance.
Market Access Teamss
Comparative evidence reviews that position devices against standard of care. These analyses feed payer dossiers, procurement tenders, and hospital decision-maker discussions.
Regulatory bodies and health agencies
Policy and regulatory bodies need unbiased SLRs to underpin public health and reimbursement decisions e.g. IQWiG or NICE in the UK
Medical Policy Teams
Rely on SLRs to shape coverage decisions, formularies, and long-term policy guidelines.
