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Yseop AI features, pricing and GDPR (October 2026)
French software that uses neuro-symbolic AI to generate regulatory reports for life sciences, such as clinical study reports.
Per user
Pricing: Per user
Annual SaaS license based on the number of users plus setup costs, amounts not published (as of September 2026).
What is Yseop?
Yseop builds software that automates regulatory document writing in life sciences, such as clinical study reports, with neuro-symbolic AI that links every sentence to its source. It serves pharmaceutical and biotech companies with medical writing teams.
Yseop's main product, Yseop Copilot, generates content grounded in source data for regulatory submissions across the CTD pyramid, the common technical document structure used for drug approval. It integrates with Microsoft Word and Veeva Vault. Yseop states that less than 7 percent of generated content needs re-authoring and that all output requires human review before submission. The company is headquartered in Paris, with offices in Lyon and New York.
Yseop AI features and use cases
- Drafts clinical study reportsYseop Copilot writes sections of clinical study reports from study data and tables. Medical writers start from a grounded draft instead of transcribing results by hand.
- Links every sentence to its sourceFull audit trails connect each generated sentence to the underlying data. Quality and regulatory reviewers can verify statements quickly.
- Keeps output consistent across submissionsThe neuro-symbolic approach produces repeatable wording across documents and submissions. Teams get consistent language across a product's regulatory file.
What sets Yseop apart
- Focus on regulatory documents in life sciences rather than general report writing.
- Neuro-symbolic AI with sentence-level traceability to source data.
- Integrations with Microsoft Word and Veeva Vault; single-tenant cloud per client.
Where Yseop is strongest
France Available internationally
Headquartered in Paris with another office in Lyon.
Questions to ask before you buy Yseop
Yseop runs as a single-tenant cloud service but publishes no certifications or hosting region, so request security documentation and the data processing agreement, especially for clinical data. Plan for human review of every output, as the vendor itself requires. Check the fit with your document management system if you do not use Veeva Vault.
Using Yseop in the EU: GDPR and AI Act
- Data locationNot published by the vendor.
- Data processing agreementNot published by the vendor: ask for one (Art. 28 GDPR).
- EU AI ActCheck whether the AI prepares decisions about people. If not, the high-risk rules usually do not apply. The high-risk obligations apply from December 2, 2027 (Digital Omnibus).
General information with sources, not legal advice.
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Questions about Yseop
Which documents does Yseop automate?
Regulatory documents in life sciences, such as clinical study reports, across the CTD structure used for submissions.
Does the output need review?
Yes. Yseop states that all output requires human review and approval before submission.
How is Yseop priced?
According to the FAQ, as an annual SaaS license based on the number of users plus setup costs. Amounts are not published.
Yseop update historyno updates yet
No changes recorded for Yseop yet.
Changes the vendor made and confirmed user reports, each checked against the vendor's own pages. We review every tool monthly.
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