Medical Writing Automation
Increase efficiencies and productivity by automating core reporting tasks for medical writing.
Yseop Copilot automates time-consuming tasks to enable regulatory documents to be delivered faster and more efficiently.
By producing first drafts of reports like the clinical study report (CSR) and clinical trial narrative (CTN), medical writing teams can focus on scientific, more complex work.
Slash writing times from 4 hours to 4 seconds
Work natively in Microsoft Word
Access medical writer user groups from Top 15 firms
Client
Include
of the worlds top life
sciences instution
Benefits for Medical Writers
50% productivity efficiency gain. Free up your time to focus on complex, interpretative, and rhetorical activities.
Remove tedious administrative work like importing and transforming tables.
Ensure FDA & EMA Compliance. Generate content which meets reviewers standards.
Automate core regulatory documents across the clinical trial process
Clinical
Discover how our AI-based, natural language generation (NLG) platform accelerates the time it takes for drugs to get to market and eliminates the risk of human error in the data review process.
Clinical Study Report (CSR)
Clinical Trial Narrative (CTN)
Summary Clinical Safety (SCS)
Summary Clinical Efficacy (SCE)
Investigator’s Brochure (IB)
Informed Consent Form (ICF)
Preclinical
Yseop Copilot’s automation packs automate the critical chain of preclinical documents to deliver a comprehensive level of report automation for highly accurate narratives.
PK (Pharmacokinetic)
The benefits of Generative AI for Pharma
Move document development upstream to accelerate downstream
30-50% reduction in authoring time and 2-week acceleration from DBL
Each day that a new drug or vaccine gets to market sooner, it creates $1-3 Million in accelerated revenue
Tim Coleman
CIO of Medicine Development, Lilly
Clients Include