Literature and data research
Searches the main paper databases and watches for new results every day.
- New paper and trial alerts
- Retraction alerts
- Evidence scores
Biotech and drug discovery
Less paperwork, more time at the bench
PubMed and Europe PMC are scanned daily for new papers and trials, along with retractions. Every project stage carries electronic signatures and an audit trail. When national R&D notices open, you get help with the application.
Where Biotech teams get stuck
- 1Days of literature search
Designing one experiment means days of digging through papers and databases.
- 2Grant paperwork crowds out research
Finding national R&D notices and writing proposals eats into lab time.
- 3Records are scattered
Lab notes and data sit in different places, so results are hard to reproduce or report.
A day with AI colleagues
- 09:00Literature Agent
Summarised new papers and trials on the targets we watch, plus any retractions.
- 11:00Experiment design Agent
Wrote a draft SOP from the research plan. The animal and biosafety approvals needed beforehand are noted too.
- 14:00Grant Agent
Checked eligibility for a national grant closing soon and outlined the proposal.
- 17:00Data Agent
Ran the statistics on the lab data and put the results in the draft report.
Example scenes. Real work runs on your company's own data and the tools you connect.
Work areas
Research projects
Every project stage carries electronic signatures and an audit trail until the final report.
- SOP drafts
- Lab notebook export
- Animal and biosafety approvals
National R&D grants
Collects national grant notices such as IRIS and SMTECH every day and helps you apply.
- Daily collection
- Eligibility check
- Proposal drafts
Bio knowledge and data connectors
Pulls target and compound data from public databases and reads it alongside expert knowledge. Clinical data comes in too.
- Bio and drug knowledge
- Target and compound data
- Industry expert Agent
AI agents on your team
- Literature AgentPaper and trial watch
- Experiment design AgentDesign and SOP
- Data AgentStatistics and reports
- Grant AgentR&D notices and proposals
- Drug discovery expert AgentTargets and compounds
- CTO AgentR&D project review
Skills ready to use
- Literature summaries
- Paper alerts
- Experiment design
- SOP writing
- Statistical analysis
- Research reports
- R&D proposal drafts
- Approval checks
Tools and data we connect
- PubMed and Europe PMC
- ClinicalTrials.gov
- ChEMBL and PubChem plus UniProt
- openFDA and Open Targets
- IRIS and SMTECH
- arXiv and Semantic Scholar
Metrics you watch together
- Literature search timePer topic
- Grant applicationsQuarterly
- Signed reportsMonthly
- Report writing timePer project
First setup
- 1Add research areas and targets
- 2Set paper alert criteria
- 3Import SOP templates
- 4Start the first research project
FAQ
Does research data leave the company?
Source data stays in your own storage. Only the queries go to external search.
Can we trust the experiment design?
Each design comes with cited literature. The principal investigator makes the final call.
Do you manage GLP or GMP documents?
There is no dedicated GLP or GMP feature yet. For now, research projects with electronic signatures and audit trails cover it, along with document management.
Start with a template made for Biotech
Choose your industry at signup and the screens and agents match it. You can change it after setup.