AI agents that map the evidence landscape, cover every congress, and track what is coming next, so your team owns the scientific conversation.
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Scientific evidence is accelerating, but scicomm teams haven't kept pace
Signal velocity and noise are outpacing team capacity.
Clinical readouts, regulatory decisions, and competitive moves reshape the scientific narrative every week. Emerging biotechs surface faster than any team can brief them. China went from marginal to the largest origin of global pipeline and publication output in five years. The volume of signal is compounding. The teams processing it are not.
Grunt work and deep work both fall on the same people.
Your team spends weeks analyzing conference readouts, pipeline movements, and investor reports to assemble one publication or congress briefing. The tools provide raw ingredients but do none of the synthesis. PoS, endpoint specifics, competitive positioning: the nuances that determine narrative quality take hours to synthesize for a single asset.
Whoever shapes the narrative first owns the scientific conversation.
And while your team is still assembling scientific briefings, nimble competitors are already publishing, presenting, and briefing KOLs. When a narrative window closes, there may not be another. Compressed timelines force decisions on incomplete work, raising the risk of losing narrative ground or missing scientific nuance entirely. A delayed story is a lost opportunity.
You define the objective. Each agent delivers a finished workflow: an evidence gap map, a congress readout, a catalyst forecast, or an MSL synthesis. Every output is cited, formatted for committee review, and exportable to PowerPoint, Excel, or PDF.
Every agent pulls from preclinical, clinical, commercial, and regulatory sources. Your methodology encodes the plan; the agent runs the workflow against it and cites every claim to source.
You validate the output, refine the plan, iterate. Agents handle the grunt work. You own the deep work.
Agent Suite for Scientific Communications
1
Evidence Gap Analyzer
Maps the published evidence landscape against your scientific story. Shows the white spaces and who is filling them.
2
Conference Coverage
Turns every congress into structured readouts: abstracts, sessions, KOL quotes, and competitor moves, ready in 24 hours.
3
Catalyst Tracker
Forecasts what is coming next: readouts, label decisions, and milestones across the competitive set.
4
MSL Insights Synthesizer
Synthesizes MSL notes, ad boards, and KOL chats into themes and sentiment shifts you can brief leadership on.
5
Custom
Build a custom agent for your workflow.
6
KOL Analytics
Profiles every expert in your space across pubs, trials, congresses, and guidelines. Tiers influence and flags rising stars.
7
AI Citation Monitor
Shows how OpenEvidence and other clinical AI tools cite the evidence in your space. Flags errors and recommends fixes.
8
Publication Impact
Measures what your publications actually moved: guidelines, altmetrics, share of voice, and clinical practice.
9
Publication Comparables
Benchmarks competitor pub strategies: which journals, formats, timing, and reach are working in your space.
Built around how Scientific Communications teams actually work
Workspace
Plan
Your methodology, encoded as steps. Review it before every run.
Output
The finished deliverable, produced by running the plan.
Chat
Ask follow-ups against any output. No rerun required.
Output
Citations
Every claim traced to source.
Export
PPTPDFXLSWEBEMAILReview-ready, share-ready.
Enterprise
Security
SOC 2 certified.
Single source of truth for every asset, trial, publication, and KOL
Data Sources
Clinical Trials211K
Pipeline Pages16K
Conferences489K
Publications246K
Regulatory4K
News264K
Investor Reports84K
China2K
Structured Tables
Landscape129K
Clinical Trials35K
Catalyst Events44K
Readouts75K
Publications2K
Share of Voice4K
KOLs
Core Entities
Clinical / Commercial Drugs23K
Preclinical Assets16K
Organizations10K
Therapeutic Areas55
Diseases13K
Indications37K
Clinical Trials35K
KOLs
The integration layer you shouldn't have to be
Most platforms make you the integration layer. One database for trials, another for publications, a third for regulatory signals, hours spent stitching them together. Ferma resolves every data point to a core entity, so clinical results, publication history, and competitive narrative context all link at the asset level. One query, full picture.
The entire platform is shaped by industry practitioners
Ferma's agents aren't built by engineers guessing what Scientific Communications teams need. They're co-designed with practitioners who have led publication plans and congress strategy at the world's largest biopharma companies.
Which data to pull, how to weight it, what thresholds matter, when to flag a risk. The implicit judgment that lives in your team's heads, made explicit and encoded into every agent.
What practitioners shape
Evidence gap criteria
How to map published evidence against a scientific story, surface white spaces, and score where your team can lead.
Data source priorities and analytics
Which endpoints matter for a given TA. How to structure a publication comp. What drives an audience reach model.
Forecasting models
Epidemiology inputs, audience reach benchmarks, narrative adoption curves, and PoS by phase. Validated against real publication and congress outcomes.
Stakeholder-ready output
Scoring dimensions, report structures, and deliverable formats that mirror how stakeholders actually make decisions.
Intelligence that compounds with every use
Knowledge stays when people leave. Every watchlist, evaluation, and annotation becomes shared institutional memory. New scicomm team members inherit years of context on day one.