Instem is proud to be exhibiting at the 47th Annual Meeting of the American College of Toxicology (ACT), bringing together the toxicology community to explore the latest developments in safety assessment and regulatory science.
Visit us at Booth 407 to meet the Instem team and discover how our solutions are helping organisations advance toxicology research, streamline workflows, and support confident regulatory decision-making.
Presentation & Symposium
Exhibitor-Hosted Program: Not Necessarily Validated: What Makes NAM Data Reviewable
As New Approach Methodologies (NAMs) become increasingly important in regulatory science, what makes the resulting data truly reviewable?
FDA’s 2026 draft guidance identifies four validation features, yet data integrity and transparency remain critical considerations for regulatory review. This session will explore what reviewers need to be able to reconstruct from NAM data and how initiatives including Complement-ARIE, VQN, and NHPig are responding through the development of data standards.
Presenter: Szczepan Baran, Chief Scientific Officer, Instem
Date: Sunday, 15 November 2026
Time: 12:00–12:55 PM
Location: Grand Oaks Ballroom, Level 2, Suite Q
Lunch will be provided.
Symposium: Safety Assessment of Extractables and Leachables under the New ICH Q3E Guideline
Join us for our symposium exploring the evolving approach to the safety assessment of extractables and leachables under the new ICH Q3E Guideline. The session will bring together a range of expert speakers, including Dr Candice Johnson, to share insights and perspectives on this important area of regulatory toxicology.
Visit Us at Booth 407
Throughout the meeting, you’ll also have the opportunity to explore Instem’s Study Management, Regulatory, and In Silico solutions and speak directly with our experts about your current research and regulatory challenges.
Provantis®
Streamlines end-to-end workflows for preclinical study management. Ask about our new Non-GLP Pathology module!
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.
KnowledgeScan™
Technology-enabled Target Safety Assessment service enabling researchers to make smarter, faster, data driven decisions.
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!
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.
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
