Instem Announces Expanded Capabilities and Increased Market Demand for Cyto Study Manager Software

Instem, a leading provider of IT
solutions to the global life sciences market, is pleased to announce
continued demand for its unique Cyto
Study Manager (CSM) genetic toxicology software solution.

CSM integrates data acquisition, auditing, reporting and study
management processes into a single intuitive system that greatly
improves efficiencies, while ensuring data integrity during genetic
toxicology studies. CSM includes modules for the comet assay,
micronucleus, chromosome aberrations as well as a revolutionary
customizable module.

Demand for CSM continues to grow and many leading R&D organizations
including Roche, Charles River Laboratories, Merck & Co., Sanofi,
Boehringer Ingelheim and, most recently, Integrated Laboratory Systems,
have selected CSM to help them streamline genetic toxicology study
workflows, reduce costs, increase efficiencies and improve regulatory

Building on this continued success, Instem has made further significant
investments in the CSM solution. Extensive reporting capabilities enable
clients to create customized reports in seconds, complete with data
tables, statistics and graphs. Instem now provides CSM validation packs,
onsite assistance and implementation support services, which are all
enabling clients to get into live use quicker and with less effort than
ever before.

Gregor Grant, Executive Vice President Preclinical Solutions, Instem,
said “It is extremely exciting to see the CSM community continuing to
grow and our clients are telling us that CSM delivers dramatic
efficiency gains within their genetic toxicology operations. Our recent
investments in the product have revolutionized the creation of genetox
reports, introduced new custom reporting capabilities, and now, by
supporting specialty assays, CSM continues to handle all genetox study
workflows and experiments.”

For further information about Cyto Study Manager download
the fact sheet or read
the case study

About Instem

is a global provider of leading software solutions and services that are
helping over 500 clients bring their life enhancing products to market
faster. We enable clients in the life sciences to more efficiently
collect, analyze, report and submit high quality regulatory data, while
maintaining compliance for their products around the world.

solutions are in use by customers worldwide, meeting the rapidly
expanding needs of life science and healthcare organizations for
data-driven decision making, leading to safer, more effective products.

supports its global roster of clients through offices in the United
States, United Kingdom, France, Japan, China and India.

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