Preclinical Document Automation
We transform your complex study data into clear, regulatory-compliant documents
Yseop Copilot's automation packs automate the critical chain of preclinical documents to deliver a comprehensive level of report automation for highly accurate narratives.
Purpose-Built for Preclinical Scientific Writing Requirements
High quality first drafts of Preclinical Reports
At Yseop, we understand the ever-evolving regulatory requirements across preclinical scientific writing. With writers facing mounting deadlines and pressure to deliver multiple studies across a growing number of molecules in the drug discovery pipeline, Yseop Copilot accelerates the delivery of drugs to market, reducing costs and impacting lives.
Yseop Copilot was designed to automate the critical chain of preclinical documents required as part of the drug lifecycle. Each automation pack:
Automation packs for the pharmacokinetic, pharmacodynamic and toxicology reports augment the delivery of regulatory documents. Simply start the process with the import of the protocol and preclinical study data, and the automation packs utilize symbolic and machine learning techniques to create a high-quality first draft.
The benefits of deep learning models
Impact: additional productivity gain + disruption in TTM gain due to full workflow automation
Firms are Leading
At the forefront of innovations and developments in AI and NLG.
Talk to One of Our Experts
Let’s start automating your data to narratives today!