Koneksa
Koneksa is a leading digital biomarker company for the pharmaceutical and biotechnology industries, specializing in developing, testing, and validating digital biomarkers to help clients understand the impact of their treatments on patients. Founded in 2013, Koneksa provides end-to-end remote clinical trial support, leveraging digital health technology, therapeutic expertise, and rapid patient-friendly remote data collection to gain better insights into patient health. Their validated, novel data algorithms are ready to deploy in treatment development programs, enabling the identification of signals earlier and faster than traditional measures. Koneksa's cloud-based SaaS platform allows multiple endpoints to be fed in real-time, giving immediate access to data and empowering confident, cost-saving decisions early in trials. The platform's ability to collect high-volume remote data with increased frequency offers ecologically valid measures and opportunities to reduce sample size.
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IXRS®3
Available in multiple modalities, our market-leading solution for patient randomization and trial supply management is the most configurable and customizable Interactive Response Technology available. From Phase I through to IV, simple designs to complex adaptive trials, IXRS®3 will easily accommodate any permutation of study objectives, and with it comes a team of professional biostatisticians, language and integration experts who are at the ready 24/7. The site-facing functions are designed to automate steps that are prone to human error. Site users have the freedom to make data corrections without the need to call a Help Desk for support or fear of deviating from trial compliance. Easy-to-read visual tools instead of hundreds of pages of specifications and legalese. View and react to each stage of the software build along the way, eliminating delivery surprises.
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BizNet
Sarjen delivers an AI-enabled Clinical Trial Management System and Bioanalytical LIMS that drives digital transformation across early-phase and late-phase clinical trials. This integrated eClinical platform supports end-to-end trial management, site management, subject tracking, regulatory compliance, and real-time laboratory sample management within a unified ecosystem. Built for pharma, biotech, and CRO organisations, the software enhances operational efficiency through workflow automation, centralised data management, and advanced analytics. Its AI features include predictive enrollment forecasting, risk-based monitoring insights, anomaly detection in lab data, automated query resolution, and intelligent dashboards that improve decision-making. By leveraging machine learning and smart automation, the platform accelerates study timelines, improves data quality, ensures compliance readiness, and transforms clinical research operations!
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PASS
PASS software provides sample size tools for over 1100 statistical test and confidence interval scenarios - more than double the capability of any other sample size software. Each tool has been carefully validated with published articles and/or texts. Get to know PASS by downloading a free trial, viewing the video to the right, or exploring this website. PASS has been fine-tuned for over 25 years and is now the leading sample size software choice for clinical trials, pharmaceuticals, and other medical research. It has also become a mainstay in all other fields where sample size calculation or evaluation is needed. In PASS, you can estimate the sample size for a statistical test or confidence interval in a few short steps. If you need guidance during any of the steps, PASS has excellent documentation, there are free training videos, and you can contact our team of Ph.D. statisticians.
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