17/02/2026
🚀 New Article Published! Unlocking the Power of Non GLP Preclinical Studies in Drug Discovery
Before a molecule becomes a drug candidate, it must survive one of the most challenging stages in R&D: preclinical evaluation. And this is where non GLP preclinical studies become true game changers.
In our latest article in Laboratory Animals journal, we highlight how early ADME tox studies—flexible, fast, and cost effective—empower teams to:
✨ Screen more candidates in less time
✨ Identify risks before they become expensive failures
✨ Make smarter go/no go decisions
✨ Select the strongest lead with confidence
✨ Reduce animal use by prioritizing in vitro models
These exploratory studies provide a competitive edge, helping organizations optimize resources while increasing the likelihood of success in later development phases.
Backed by insights from the Preclinical Area at Fundación MEDINA, the article also showcases companies offering ready to use models and on demand assays to accelerate discovery.
If your work touches early drug development, pharmacology, biotech innovation, or strategic R&D decisions… this is a must read.
https://www.medinadiscovery.com/wp-content/uploads/2026/02/Preclinical-Studies-and-GoNo-Go-Decision-Criteria-in-Early-Drug-Development.pdf
👉 Elevate your pipeline. Reduce risk. Accelerate innovation.
-tox SECAL, Sociedad Española para las Ciencias del Animal de Laboratorio Confederación de Sociedades Científicas de España (COSCE) Universidad de Granada MSD España Junta de Andalucía