Frequently Asked Questions (FAQ's)
Puraite is an AI-powered platform that automates and accelerates systematic literature reviews (SLRs) and related evidence synthesis workflows. We combine scientific rigor with explainable AI (XAI) to deliver transparent, reproducible, and regulatory-compliant results for the life sciences and healthcare industries.
A SLR is a structured process to identify, assess, and synthesize all relevant studies on a specific research question. It is the gold standard for evidence generation in healthcare, regulatory, and HTA contexts.
Our primary users are pharmaceutical and medtech companies, contract research organizations (CROs), health technology assessment (HTA) bodies, and public research institutions in academia. Puraite is designed for anyone who needs reliable, large-scale evidence synthesis to support regulatory submissions, market access, or informed, scientific decision-making.
Most competing tools operate using black-box LLMs, which creates risks in regulated environments. Puraite is unique because it provides: - Full transparency and audit trails through advanced verification layers that transform AI black boxes into transparent, human-verifiable white boxes - Accuracy levels exceeding 95%, matching or surpassing human researcher performance - Seamless integration with established reporting standards such as PRISMA, Cochrane, and JCA requirements - Direct access to one of Europe’s largest supercomputers, ensuring the computational power required for high-quality, automated evidence synthesis
Yes. Our models are benchmarked against Cochrane gold-standard datasets and validated in pilot projects with leading pharma companies and CROs. We are committed to peer-reviewed validation and transparent performance reporting.
No. Puraite augments expert reviewers by automating repetitive and time-consuming steps. Human oversight remains essential for protocol design, interpretation, and final decision-making. Our philosophy is 'AI-assisted, human-validated'. We believe that a human-in-the-loop approach is the way forward.
Currently, Puraite supports systematic literature reviews. Our roadmap includes support for scoping reviews, rapid reviews, umbrella reviews and network-meta analyses.
We adhere to strict data security and compliance standards, including GDPR. Data can be hosted in secure EU-based servers at our premises, and custom deployments (e.g., on-premise or private cloud) are available for enterprise clients.
All data can be exported in standard formats (RIS, CSV, XML, JSON) and aligned with PRISMA flow diagrams, HTA submission templates, and publication-ready outputs.
Our pricing depends on project scope and user needs. We offer flexible subscription tiers billed per user per month and enterprise licensing, designed to scale with your review volume and team size. No cost for academic partners and NGOs.
Yes. Puraite integrates with commonly used reference managers, statistical tools, and regulatory reporting formats. API access is available for advanced workflows and enterprise clients.
Yes. Our technology also supports applications in public health, guideline development, and policy-making, as well as industries like nutrition, cosmetics and MedTech.
You can request a demo or pilot project with our team. Simply contact us via our website or email. We typically begin with a pilot project where we apply Puraite to one of your previous reviews to demonstrate efficiency gains and regulatory compliance.
Our Funding Partners
Puraite has secured more than €1.1 million in non-dilutive financing through highly competitive German funding programs, including Startup Transfer.NRW and EXIST Transfer of Research.
Co-funded by the German Federal Government and the European Union, these programs are specifically designed to support breakthrough innovations at the interface of academia and industry and are awarded only to a very limited number of high-potential Deep Tech teams.




Puraite – Real-Time Medical Evidence
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