Research Platform · Beta
Abkus Academic
An AI-powered research management platform for scientists, researchers, and institutions. From regulatory guidance to grant discovery to publication-ready outputs — the complete research lifecycle in one system.
Free during beta
Abkus Academic is currently free for all researchers during the beta phase. Plans start at $19/month when billing is activated.
Who uses Abkus Academic
- ✦ Academic researchers at universities seeking regulatory approval for innovations
- ✦ R&D teams at pharmaceutical, medtech, and biotech companies
- ✦ Graduate students and postdocs managing systematic literature reviews
- ✦ Technology Transfer Offices (TTOs) at universities and research centers
- ✦ Institutional research boards requiring compliance traceability
The problem it solves
- ✦ Researchers spend 40%+ of time on regulatory paperwork — mostly manual and repetitive
- ✦ Grant opportunities are missed because discovery is fragmented across dozens of portals
- ✦ Literature reviews take months; PRISMA compliance is error-prone without tooling
- ✦ Technology transfer knowledge is siloed, delaying commercialization
All capabilities
Regulatory Guidance
AI classification for ANVISA, FDA, and EMA. Receive a personalized approval roadmap with required documentation, compliance steps, and estimated timelines for your product category.
Systematic Literature Review
Search PubMed, Embase, and major academic databases. Generate PRISMA-compliant systematic reviews and export to DOCX, LaTeX, Markdown, or PRISMA diagram format.
Grant Discovery
Find compatible funding from NIH, NSF, CAPES, FINEP, CNPq, FAPESP, and 40+ agencies. AI analyzes grant-project fit and drafts proposal sections tailored to each call.
Technology Transfer
Analyze patent landscape, licensing pathways, and spin-off potential. Understand the commercialization routes available for your research output.
Technical Dossier
Build your CTD (Common Technical Document) module by module. AI drafts each section based on your project data, following ANVISA/FDA/EMA submission standards.
Team Collaboration
Invite co-researchers, assign roles, and collaborate on projects in real time. Admin subscribers can add team members within their plan scope.
Document Management
Centralize all research documents — protocols, ethics approvals, data files, regulatory submissions — in one project workspace with version tracking.
Regulatory Monitoring
Automatic alerts for ANVISA, FDA, and EMA regulatory updates relevant to your product category. Never miss a compliance deadline or a new guidance document.
Project Reports
Generate progress reports across all research phases — from literature review to regulatory submission — with a single click. Share with advisors or institutional boards.
Discovery & Benchmarking
Search across the research ecosystem to find similar projects, identify collaboration opportunities, and benchmark your research against comparable initiatives.
Multi-Agency Dossier Comparison
Compare what each agency (ANVISA, FDA, EMA) requires for the same product. Understand jurisdictional differences and plan your global regulatory strategy.
Activity & Audit Log
Full traceability of all research actions — who did what and when. Essential for GCP/GLP compliance and institutional audit requirements.
Pricing
Free during beta. Plans activate when billing launches (~Q3 2026).
Researcher
$19/month
Individual researchers and academics
- ✓2 projects
- ✓3 team members
- ✓All AI features
- ✓Literature review exports
Lab
$29/month
Research labs and study groups
- ✓5 projects
- ✓10 team members
- ✓Priority AI processing
- ✓Advanced grant matching
Institution
$79/month
Universities and research institutions
- ✓Unlimited projects
- ✓Unlimited members
- ✓Custom regulatory workflows
- ✓Dedicated support
Start researching today
Free during beta. No credit card required.