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

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)

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

We wanted to be certain and very accurate around what we produce in these documents that are submitted to health authorities. We want to deliver a draft through Artificial Intelligence that is 100% reliable and needs no further editing by human medical writers. That is what we have achieved with the Yseop collaboration.

Machine learning is a part of every aspect of Lilly’s future, from drug discovery to clinical trials to manufacturing to patient support. Yseop brings a novel approach to regulatory submissions and other reporting, and we see opportunities to bring Yseop’s technology to teams throughout the enterprise.

Equipped with instant insights and impactful visuals and texts, our finance teams can now jump into the next generation of data analytics.

Yseop enables us to focus our discussions on action plans for the branch. Now we spend more time talking about sales performance rather than analyzing figures. It saves time for myself and my team.

The Yseop engine produces this commentary in less than a second. We are just scratching the surface with this technology.

With Yseop, we give clear explanations to our customers. The customer understands the decision and I have more time to focus on other opportunities. It's a real innovation!

Talk to One of Our Experts

Let’s start automating your data to narratives today!