Blog
Keep up to date with the latest news from Instem.
The Journey of a Molecule – Toxicology
Accelerating Preclinical Safety with Connected Data and Predictive Insights
Seamless Document Control with eQCM
By unifying workflows, standardizing processes, and embedding real-time oversight, eQCM transforms document management into a controlled, transparent, and efficient system.
Webinar Recap: Advanced Colony Management with Climb™
In this recap, we cover how Climb can support robust animal management, from breeding strategies and essential housing logistics, to adverse event tracking and real-time veterinary alerts.
Challenges and Best Practices of Open-Source Solutions for Clinical Use
Read this blog to learn about the challenges and best practices when using open-source solutions in clinical trial data analytics.
The Journey of a Molecule – Preclinical Efficacy
Enhancing Study Quality and Data Integrity in the Preclinical Phase
INSTEM Announces Extension of Research Collaboration Agreement with U.S. FDA to 2031
Instem, a global leader in SaaS solutions for life sciences R&D, today announced a 5-year extension of its Research Collaboration Agreement (RCA) with the U.S. Food and Drug Administration (FDA).
Implementing R in Modern Life Sciences: Managing Risk and Ensuring Compliance
In this blog, we answer a number of recurring questions about validation, reproducibility, governance, and risk while using R for clinical data analytics.
The Journey of a Molecule – Lead Optimization
Unifying Science and Safety to Navigate the Iterative Path of Lead Optimization
The Case for Outsourcing EU CTR, Policy 0070 & HC Submissions
In this blog, we discuss the need to outsource CTT work for EU CTR, Policy 0070 & HC Submissions as pharma cuts back on internal CTT teams.
