ClinIAMind helps consultants, SMEs, and Regulatory Affairs teams centralize PDFs, search smarter, annotate faster, and generate structured evidence workflows for IVDR and other literature-heavy healthcare projects.
No credit card required · Built for consultants, SMEs & Regulatory Affairs teams
Less time spent on literature review
PDFs analyzed per project
Full audit traceability
Always available
ClinIAMind transforms disconnected PDF collections into a structured, searchable knowledge workspace designed for evidence-heavy projects.
Set up a dedicated workspace for a product, topic, or regulatory file. Drag and drop your publications — the AI instantly extracts metadata and indexes everything for semantic search.
Drop your PDFs here
High sensitivity RT-PCR detection of SARS-CoV-2...
Lancet · 2023
Comparative analysis of molecular diagnostics...
NEJM · 2023
Systematic review of IVD diagnostics for COVID...
BMJ · 2022
Use semantic search to find the most relevant information across your document set faster. No more boolean keyword frustration — ask in plain language and get sourced answers.
Highlight a passage and the AI generates a structured annotation with the relevant regulatory context. All your findings stay centralized, traceable, and ready to export.
Sensitivity 97.3% and specificity 99.1% — excellent performance for Class C IVD device. Relevant for SVR report section 5.2.
Generate outputs that help support scientific summaries, evidence reviews, and regulatory documentation tasks — including structured SVR, PER, and PMS reports for IVDR workflows.
No long onboarding, no technical complexity. Start analyzing your publications in under 5 minutes.
Set up a dedicated workspace for a product, topic, scientific question, or regulatory file.
Use semantic search to surface relevant findings faster. Capture key evidence with AI-assisted annotations.
Generate reusable outputs — SVR, PER, PMS reports and structured summaries ready for scientific and regulatory documentation.
Consultants, SMEs, and Regulatory Affairs teams share their experience with ClinIAMind.
“The semantic search is a game changer. What used to take me two hours of PubMed browsing now takes a few minutes. And the AI annotations save me an enormous amount of manual work.”
Regulatory Affairs Consultant
Independent practice
“We were preparing an IVDR submission with a very tight deadline. ClinIAMind helped us structure our evidence in a fraction of the time. The traceability alone is worth it.”
Regulatory Affairs Manager
MedTech SME
“I manage several client projects at once. Having everything centralized by project, with annotations I can actually reuse, has completely changed how I work.”
Scientific Affairs Consultant
Healthcare consulting
ClinIAMind is the AI-powered literature intelligence platform for consultants, SMEs, and Regulatory Affairs teams working on evidence-heavy healthcare projects.
A practical workspace for handling multiple client literature projects, accelerating review, and delivering more traceable work.
Key features
Reduce time spent manually scanning PDFs and locating relevant information.
Keep a clear connection between your conclusions and the underlying publications.
Organize projects, annotations and outputs in a more standardized way.
A productivity layer for literature-intensive regulatory preparation.
Start with a free project, then scale as your literature and documentation workflows grow.
* Prices exclude tax. VAT will be calculated automatically based on your country at checkout. European businesses with a valid VAT number benefit from reverse charge.
Start with a free project and see how ClinIAMind can help your team work faster, stay organized, and build more traceable documentation workflows.