Why Scantox as your preferred CRO?
Our services support a broad spectrum of preclinical drug development elements. From lead optimization within in vitro and in vivo efficacy models, formulation development, regulatory toxicology studies incl. supportive functions as clinical pathology, bioanalysis, histology all the way to manufacturing and distribution of products for clinical trial phase 1 and 2.
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our next webinar
The Scantox webinars are free to attend, and a great opportunity to gain scientific insights from our subject matter experts.
Addressing Genetic Toxicology Assessments Across Screening, Regulatory Stages, and Beyond
Date: December 10, 2025
Time: 15:00 CET | 9:00 AM EST
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Sustainability is built into how Scantox operates – from how we source energy and manage facilities to how we train, report, and collaborate. Our approach balances scientific rigor with ethical responsibility, offering measurable impact to the clients we serve.
Shape the Future with Scantox
At Scantox, your background doesn’t define your future. We offer meaningful projects, real impact, and space to grow wherever you start.
We’re looking for empathetic, passionate people who take initiative, embrace challenges, and aim to make a difference.
Join Scantox Group and help shape the future for patients worldwide.
