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Enterprise Layer Intelligence
Categories/Healthcare & Life Sciences/Peer AI
Peer AI

Peer AI

Founded 2023

Draft life sciences regulatory submission documents and predict reviewer questions before filing

Pricing model

Demo

You can use Peer AI to author regulatory documents and manage submission workflows across life sciences programs. It provides specialized agents that generate first drafts for pre-clinical, CMC, and clinical documents like protocols, IND modules, and safety narratives. You can track every output back to its original source data tables, maintain full audit trails, and keep institutional knowledge inside your team. The system also predicts questions regulatory reviewers might ask so you can fix gaps before submitting. You can monitor program bottlenecks and manage team review cycles directly.

What Peer AI does

Draft clinical study report summariesGenerate patient safety narrativesReview documents for regulatory inspection readinessTrace claims back to source data tablesIdentify program bottlenecks and review delaysExport regulatory documents formatted to company templatesSpecialized writing agents for preclinical, CMC, and clinical documentsPredicts questions that regulatory reviewers are likely to askComplete data traceability linking generated text back to raw source tablesIdentification of project bottlenecks and dependencies across filing programsCustom alignment with organization templates and style guidesDeployment options for private cloud or internal AWS environmentsStrict zero data retention policies to prevent training on sensitive data

Pricing breakdown

Pricing model: Book a demo

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Peer AI, regulatory submissions, medical writing, clinical study reports, IND modules, protocol drafting, safety narratives, life sciences, regulatory affairs, document traceability, agentic writing, biopharma compliance, FDA submissions, audit trail, clinical documentation