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🚀 Sorcero raises $42.5M Series B funding to transform medical-led commercialization in life sciences. Learn more
Sorcero SciComms™

Scientific communication.
Reimagined.


From content generation to publication intelligence.
Turn complex science into impactful narratives.

Timelines are shrinking. Audiences are growing. Sorcero SciComms bridges the gap with the world’s most advanced medically-tuned AI.

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Proven impact.


Redefining the speed and standard of scientific communication.

Days

instead of months.

From source to
manuscript draft.

18x

higher engagement.

From patient &
non-specialist PLS.

250M+

publications.

Continuously ingested
and enriched.

The SciComms engine for every stage.


Sorcero SciComms™ doesn’t just summarize text. We power your entire pipeline.

Discovery

Build your strategy on a foundation of
total visibility.

Publication Intelligence

Align with evolving narratives using the industry’s largest repository of 250M+ publications.

Gap Analysis

Instantly identify evidence gaps to inform R&D priorities.

Lexicon Development

Establish core product narratives early.

Congress Materials

From complex source data to congress-ready
deliverables.

Abstracts

High-quality, SME-reviewed standards produced faster than manual drafting.

Posters

Deeply structure drafts including detailed design for figures and tables.

Oral Presentations

Rapid generation of core narratives grounded in verified source evidence.

Manuscripts

From unstructured source data to a
high-quality manuscript draft in days.

Phase I (Safety) (Coming soon)

Diverse data (Safety, PK/PD, preliminary efficacy) synthesized into coherent narratives.

Phase III (Superiority, Non-Inferiority)

Large-scale, complex datasets around primary and secondary endpoints structured in full adherence to CONSORT 2025 guidelines.

Secondary (PRO, Subgroup analyses)

Capture the patient perspective in compliance with CONSORT-PRO.

Publication Extenders

Broaden the reach of your science, helping
patients and stakeholders understand the
science behind the treatments being developed.

Plain Language Summaries (PLS)

Peer-reviewed validated PLS that meets journal requirements andstakeholder expectations.

Video PLS (vPLS)

Generate high-quality, compliant, reach-enhancing videos in a timely and cost-effective way.

Plain Language Trial Summary (PLTS)

Includes all 11 mandatory elements required by EU CTR 536/2014, Annex V.

Regulatory & Market Access

Speak the language of regulators and payors.

HEOR Narratives (coming soon)

Generate economic evidence narratives that resonate.

Regulatory Submissions

Ensure consistency across submission documents.

A new standard for scientific
content generation.


Manuscript Drafts

From source to delivery in less than a week.

Reduce Time-To-Publication with foundational drafts that are ethically compliant, scientifically accurate, and structurally complete.

Plain Language Summaries

Science for everyone.

Break down barriers to patient engagement. Transform how you create compliant PLS, exceeding FDA and EMA readability standards.

 

Quality you can trust.

Validated by industry leaders. We established a rigorous scoring rubric with 3 top-ten pharma companies and leading agencies.

Sorcero combines Agentic AI with mandatory Subject-Matter-Expert (SME) review to ensure unparalleled speed and scientific integrity.

   Scientific Accuracy

   Non-negotiable checks for data integrity and protocol fidelity.

   Content & Completeness

   Ensuring all IMRAD components and mandated elements are present.

    Polish & Professionalism

    Assessing flow, tone, and clarity.

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Publication Intelligence.
Crystal clear.

 
Sorcero Publication Intelligence bridges the gap between global scientific discourse
and your organization’s decision-making. We fuse the world’s most comprehensive
evidence base with advanced AI to transform static documents into dynamic,
actionable intelligence.

 
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Built on a better foundation.

Sorcero isn’t a generic LLM. It is the most advanced AI platform engineered specifically for Life Sciences.

Industry-Leading Compliance

Engineered to meet GPP4, ICH, CONSORT, and FDA requirements.

Data Security

Full data security with a dedicated tenant for your organization.

Massive Scale

Trained on 100M+ authors and 250M+ publications.

THE CHALLENGE

The "Publish or Perish"
Pressure Cooker

You are sitting on groundbreaking science, but the barriers to engagement are higher than ever.
Scientific research is exploding, but the teams responsible for communicating it are stretched thin.

flask

Volume Overload

The pressure to publish more is relentless, but monitoring emerging trends and massive datasets is manually impossible.

time

The Speed Trap

Converting complex clinical data into high-quality manuscripts takes months of manual writing and review.

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The Readability Gap

Despite draining time and budget, patient-facing materials often fail to meet readability standards, leaving patients and advocates in the dark.

check

Compliance Risk

Navigating evolving guidelines (CONSORT, STROBE, EMA CTR) is a complex, high-stakes minefield.

You don’t need a faster typewriter. You need a stronger pipeline.