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

Each day that a new drug or vaccine gets to market sooner, it creates $1-3 Million in accelerated revenue

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.

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.

It used to take us a minimum of 4 hours to write 1 patient narrative. Now, it takes 4 seconds to write an unlimited number of them.

Talk to One of Our Experts

Let’s start automating your data to narratives today!