Instem is proud to be sponsoring the 60th EUROTOX Congress once again this year.
Visit us at Booth 23 to discover our industry-leading solutions for preclinical study management, regulatory compliance, predictive toxicology, in silico modelling, and data-driven insights. Our team will be on hand throughout the event to discuss how we can help accelerate your research and support your scientific and regulatory goals.
Presentations & Posters
Exhibitor Hosted Event – Data a Regulator Can Act On: NAMs-Ready Infrastructure for ADME and Early Safety
Join us on Tuesday, 15 September, from 12:15–13:15 in Room 0.16 for our Exhibitor Hosted Event, presented by Szczepan Baran, Chief Scientific Officer at Instem. The session will explore the data infrastructure required to operationalise New Approach Methodologies (NAMs) across ADME, DMPK, and early safety workflows. Lunch will be provided.
Poster Presentation – An Integrated Framework for Supporting Read-Across Assessments in Chemical Safety
Visit Poster P18-120 during Poster Viewing 1 (PV01) on Monday, 14 September 2026, with viewing taking place during the coffee and lunch breaks. Presented by Mahmoud Ahmed, Research Data Scientist at Instem, the poster presents a detailed case study focusing on extractables and leachables exceeding systemic toxicity qualification thresholds under emerging regulatory guidance (ICH Q3E). The case study and overall framework illustrate how a unified, software-supported framework integrating cheminformatics, toxicological data, and structured expert input can support transparency, consistency, and scientific confidence in read‑across based safety assessment. This framework can be applied across a broad range of substance classes, regulatory contexts, and product domains.
Learn more about our leading software & services, including:
Provantis®
Streamlines end-to-end workflows for preclinical study management. Ask about our new Non-GLP Pathology module!
Logbook™
An electronic laboratory notebook (ELN) that simplifies and streamlines the digitization and documentation of lab processes.
SEND Advantage™ Outsourced Services and Consulting
A suite of services that ensure your nonclinical data meets the Standard for Exchange of Nonclinical Data (SEND) submission requirements.
Submit™ Seamless Electronic SEND Submissions
Improves the speed and quality of new pharmaceutical developments by enabling the efficient exchange of critical study data between sponsors, CROs and regulators.
Cyto Study Manager™
Enables improved management of genotoxicity studies, delivering enhanced accuracy, documentation and compliance.
Leadscope Model Applier™
An advanced In Silico toxicology tool that helps scientists predict toxicity endpoints, review results with confidence, and generate regulatory-compliant reports. Ask the team for a demo of our new Toxicity Profiler!
KnowledgeScan™
Technology-enabled Target Safety Assessment service enabling researchers to make smarter, faster, data driven decisions.
Centrus®
This powerful tool consolidates and structures data from various sources into a unified, accessible platform, enabling high-quality data management and seamless data sharing for early-stage research.
Advance™
A comprehensive solution supporting the ICH S1B Weight of Evidence Addendum for assessing carcinogenicity risk. Advance streamlines early-stage safety evaluations, reducing costs, saving valuable time, and minimizing the need for animal testing.
Predict™
Our Predict service uses advanced QSAR techniques to streamline early-stage safety assessments through predictive modeling. Enables researchers to evaluate potential toxicity risks quickly, supporting data-driven decision-making and reducing the need for subject testing.
Want to talk in more detail? Contact us to schedule a 1:1 meeting. We look forward to seeing you there!
For more information, visit the Event Website
