Safety Assessment Tools for Accurate, Confident, and Efficient Analyses
Overcome concerns about tool reliability and performance with industry-leading solutions that simplify and derisk preclinical safety assessments. Our tools help you manage data throughout the development pipeline and generate robust safety insights for confident decision-making.
Solutions to Support Safety Professionals
As a safety professional, you are responsible for conducting or overseeing target safety assessments (TSAs) early in the development process. Few roles are as critical to study success and resource efficiency, highlighting the need for reliable tools. We understand the pressures of your role and how relying on inflexible and inconsistent methods introduces needless risk and frustration into your daily work. You deserve scientifically-backed, industry-standard tools that help you:
- Generate comprehensive overviews of study data to form coherent and concise weight-of-evidence assessments
- Expand your teams while maintaining secure systems
- Accurately identify areas of risk for a compound as early as possible
We provide safety professionals in preclinical teams with a suite of tools for preclinical risk assessments and study management, helping to simplify early decision-making and strengthen project foundations.
Featured Products
Instem offer a range of products to support your important work as a Safety Professional, visit the pages below to learn more.
Provantis®
An end-to-end preclinical study management tool for GLP and non-GLP environments that enables reliable study design, execution, data analysis, and reporting.
- Accurate data integration across all study stages gives you a holistic view for more informed decisions
- Reduced data recording error improves confidence and minimizes resource misplacement
- Built-in support for diverse study designs allows you to tailor tools to your specific needs
Advance™
A single platform for carcinogenicity risk assessment, aligned with the ICH S1B Weight of Evidence (WoE) Addendum, helping you avoid costly two-year rat studies.
- Designed by experts with direct ICH S1B framework experience
- Cuts time-to-market by 3-5 years while reducing reliance on animal testing
- Strategic integration across multiple study phases supports thorough analyses
Climb™
Climb™ is a cloud-based end-to-end software solution for the management of non-GLP animal studies. This comprehensive platform comes with powerful functionalities enabling researchers to set up, schedule, manage, track, and log all in vivo projects, and access data from a centralized repository. Climb provides efficiency, accuracy, and compliance in non-GLP studies of all sizes and complexities, giving researchers confidence to make faster, data-driven decisions.
Centrus®
A centralized preclinical safety assessment platform that supports safe and efficient team expansion for growing study needs.
- Enables faster and more accurate safety assessments to reduce risk and improve resource efficiency
- Facilitates collaboration through a centralized platform with secure data sharing in standardized formats
- Accelerates development timelines by helping you identify risks early
Featured Resources
Learn more about how our solutions can impact your research through our helpful resources.
Why Instem?
Our scientific experts have helped hundreds of clients achieve successful regulatory submissions. Instem solutions have been used in every FDA submission since 2016 and are now adopted by every major CRO. We are a trusted solution for any organization aiming to maximize development efficiency while mitigating risk and ensuring compliance in early in vitro and in vivo work.
Related Products
Instem offer a wide variety of products to support safety professionals. Visit the pages below to learn more.
Get a Free Demo Today
Are you ready to streamline your preclinical studies while ensuring data integrity every step of the way? Join the leading labs worldwide that trust Provantis to deliver efficient, reliable study management solutions.
Request a demo today and take the first step towards transforming your workflows for preclinical study success.

