Download the case study to learn more about what challenges were overcome and what benefits were achieved with the deployment of Provantis.
What is Provantis?
Provantis is the industry-leading GLP-compliant preclinical study management software, supporting every study phase from design to reporting. Trusted globally by study directors and lab managers, it streamlines workflows, ensures data integrity, and accelerates regulatory submissions.
Provantis is a fully integrated solution that optimizes study design, minimizes the risk of error, and ensures compliance while providing a seamless, efficient user experience. Managing preclinical studies can be complex; poor study oversight and substantial data review may add months to a timeline, while data errors and study deviations risk the integrity of results.
As an all-in-one solution, Provantis simplifies the entire preclinical study process, from study design and data capture to analysis and reporting. By integrating workflows across study phases, Provantis improves data reliability, reduces costs, and accelerates time to submission.
Designed for both GLP and non-GLP environments, Provantis is scalable to meet the needs of individual scientists, research organizations, pharmaceutical companies, and universities. Its modular design offers full customization to meet the requirements of even the most complex studies.
Provantis provides flexible deployment options to suit your organization’s needs while supporting robust security, accessibility, scalability, and training.
The Case Study
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 modules for General Toxicology, Pathology, Clinical Pathology and Reproductive Toxicology.
Download the case study to learn more about what challenges were overcome and what benefits were achieved with the deployment of Provantis.
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