Medical writing automation

Yseop Copilot automates time-consuming regulatory writing tasks for pharmaceutical companies by producing first drafts of clinical study reports, clinical trial narratives, safety and efficacy summaries, investigator brochures, and informed consent forms.It integrates natively with Microsoft Word so medical writers can focus on scientific interpretation and higher-value work while generating compliant document drafts faster.

Eli LillyPharma

Yseop Copilot automates compliant document generation across clinical, safety, and CMC workflows directly in Microsoft Word and Veeva Vault.The platform supports regulatory writing for life sciences teams by generating source-driven drafts, live updates, and submission-ready dossiers.It covers core eCTD document types including Clinical Study Reports, Investigator’s Brochures, and Informed Consent Forms.

YseopPharma

AstraZeneca China built an adverse event summary system using Tongyi Qianwen (Qwen) on Alibaba Cloud Dedicated Model Studio.The system ingests medical literature and drafting inputs, generates adverse-event reports to regulatory standards, and requires only human review and minimal edits before sign-off.The implementation uses a private deployment for stronger data/system segregation and privacy protection.

AstraZenecaPharma