by John Gard | Feb 10, 2026 | Compliance Builder, Study Management
Organizations operating in regulated, life science environments face constant pressure to maintain data integrity, ensure system security, and meet evolving regulatory expectations such as FDA 21 CFR Part 11. By providing real-time compliance monitoring, electronic...
by John Gard | Jan 15, 2026 | Resources
Pathologists and study directors are under growing pressure to deliver high-quality results faster, without compromising accuracy or data integrity. Manual, unstructured approaches to pathology data entry and study management can no longer keep pace with the demands...
by John Gard | Jun 10, 2025 | Study Management
At Instem, we’re constantly listening to our users and converting that insight into better study management solutions. Today, we’re thrilled to share the results of those efforts. Logbook 6.6 will be released soon, and it brings with it intelligent and dynamic...
by John Gard | Jun 3, 2025 | Provantis, Study Management
Accelerate Your Formulation and Dosing Workflow Accurate and traceable information for reagents, test items, and formulations is crucial for meeting regulatory standards and maintaining research integrity in preclinical toxicology studies. As these studies grow in...
by John Gard | May 5, 2025 | Provantis, Study Management
In the world of scientific research, especially within preclinical laboratory settings, managing vast amounts of data and ensuring the integrity of that data is crucial. For research organizations, pharmaceutical companies, and other research facilities, a Laboratory...
