AI drafting and QC in Microsoft Word
Publications and Congress Abstracts
A congress abstract has to fit the key results into a few hundred words, under the congress rules. PharmAssist drafts it from the approved outputs and cites every number.
See Publications & abstracts drafted in Word
A short demo on a fictitious study and product. In a live demo we walk through the same workflow and answer your questions about sources, review and deployment.
Read the transcript
A congress abstract has to fit the key results into a few hundred words, under the congress rules. PharmAssist works inside Word. Choose the document type and add your source files. It lays out the document's outline, right in Word. Pick a section, and PharmAssist drafts it from your sources. Review the draft, then insert it into your document. You can also ask questions in chat. Answers come from your own files, and show which ones they used. From your sources to a draft in Word, ready for expert review. Book a demo at gentext.ai/pharma.
Can AI write a congress abstract from study results?
Yes, as a sourced draft for authors to review. PharmAssist drafts the abstract or manuscript sections from your approved CSR and statistical outputs, within the word limit and structure the congress or journal sets, and cites the source for every result. Authors keep control of interpretation and authorship, in line with your publication policy.
How this document gets written today
Publication teams turn approved study results into abstracts, posters and manuscripts on tight congress deadlines, with strict word limits and structures.
Every number must match the approved outputs, and authors need to see where each claim comes from before they sign off.
What your team can work on
The selected congress or journal structure, applied in line with your publication policy and Good Publication Practice.
Abstract drafts
Draft background, methods, results and conclusions within the congress structure and word limit.
Manuscript sections
Draft methods and results sections from approved outputs for author review.
Evidence reconciliation
Every result cites its table or report section.
Requirement checks
Check structure and length against the requirements you supply.
How it works for Publications & abstracts
Choose abstract or manuscript
Select the publication type and the target congress or journal.
Add outputs
Upload the CSR, statistical outputs and the requirements.
Draft and check
Draft and review citations and requirement checks.
Author review
Insert into Word for author review and approval.
What it drafts from
Select the approved sources for the task. Data handling follows the deployment and model-service configuration agreed with your team.
- Approved study reports and statistical outputs
- Publication plan
- Congress or journal requirements
What stays with your team
PharmAssist supports your document workflow. Interpretation, medical and regulatory judgement, approval and submission stay exactly where they are today, with qualified people and your existing review chain.
Choose GenText-hosted SaaS or a private deployment. Confirm access, data handling, model services and retention during supplier qualification.
Security and deployment detailQuestions we are asked about this document
Does AI-assisted drafting fit Good Publication Practice?
Your publication policy decides how AI assistance is disclosed. PharmAssist keeps every statement tied to approved sources and leaves interpretation and authorship to the authors.
Can it keep to a word limit?
Yes. Drafts follow the structure and word limit you supply, and the check shows the length.
Can it draft plain language summaries too?
Yes. See the plain language summaries page.
Who reviews and approves the Publications & abstracts?
Your qualified specialists do. PharmAssist drafts and checks; scientific interpretation, medical and regulatory judgement, quality review and approval stay with your team and your existing review chain. Open questions and missing inputs stay visible in the draft until a person resolves them.
Does PharmAssist work inside Microsoft Word?
Yes. PharmAssist is a Microsoft Word add-in for Windows, Mac and Word on the web. You choose the document type, add your source files, review the outline and section drafts in a side pane, and insert approved text into the document you are already working on.
Where does our data go, and do we need a Veeva connection to begin?
Choose GenText-hosted SaaS or a private deployment. Data handling, model services and retention are confirmed with your technical owner during supplier qualification. A demonstration starts with fictitious documents and upload; connections to Veeva Vault or other source systems are scoped during implementation.
Teams that start here often widen to
Scientific communications
Plain Language Summaries
Tell patients and the public what a study found, simply.
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Clinical trial documents
Clinical Study Reports
Draft ICH E3 CSR sections where every number matches the tables.
Read more
Real-world evidence
Real-World Evidence Protocols and Reports
Draft non-interventional study protocols and reports.
Read more
Talk to us about Publications & abstracts
Tell us your role, source material and next document milestone. We will confirm the demonstration scope and define a paid pilot with your team.
Prefer email? alex@gentext.ai