by Instem Team | Feb 25, 2025 | Regulatory Submission, SEND
A thorough guide to this new SEND standard to help your team be prepared. On March 15, 2025, the Standard for Exchange of Nonclinical Data (SEND) Implementation Guide Genetic Toxicology version 1.0 (SENDIG-GeneTox v1.0) will become a regulatory requirement for in vivo...
by Instem Team | Feb 24, 2025 | Resources
Learn How to Combat the Major Obstacles When Building or Growing a Biostatistics Team There can be many hurdles to overcome as a new or growing Biostats team. From validation burdens to access mismanagement to audit preparedness and much more, new and growing biostats...
by Instem Team | Feb 24, 2025 | Resources
Is your team ready for SENDIG-GeneTox v1.0? On March 15, 2025, the SEND Implementation Guide for Genetic Toxicology version 1.0 (SENDIG-GeneTox v1.0) will become a regulatory requirement for in vivo genetic toxicology data submissions to the FDA. For a detailed...
by Instem Team | Feb 9, 2025 | Resources
Replace GLP and Non-GLP Paper Data Logbook™ is helping clients across the globe reduce and even eliminate the vast number of paper forms that are used in their laboratories, resulting in reduced costs, increased efficiencies, and improved...
by Instem Team | Jan 17, 2025 | Resources
Provantis Integrated Preclinical Software SRI Biosciences Reduced Costs, Improved Compliance, and Increased Growth Contract Research Organization, SRI Biosciences, needed a robust preclinical software solution and implemented Instem’s Provantis suite, including...
