AI Document Solutions for MedTech & BioTech
AI-powered document generation for clinical evaluation reports, regulatory submissions, risk assessments, and medical writing.
AI Clinical Evaluation Report Generator
Draft EU MDR-compliant Clinical Evaluation Reports with AI. Vespper connects your clinical data, literature, and PMS records into structured, traceable CERs.
AI Regulatory Submission Writer
Draft FDA 510(k) submissions, EU MDR technical files, and regulatory documents with AI. Full traceability from source data to final submission.
AI Risk Assessment Writer
Generate ISO 14971 and ISO 12100 risk assessments with AI. Traceable hazard analysis mapped to mitigation measures and documentation requirements.
AI Document Editor for Regulatory Affairs Teams
The AI document editor built for regulatory affairs. Draft submissions, maintain technical files, and produce audit-ready documentation with full traceability.
AI Document Editor for Medical Writers
The AI document editor built for medical writing. Draft CERs, CSRs, and regulatory submissions with clinical data traceability and structured output.
