Services
Chellsy delivers sophisticated solutions for conducting diverse observational research methodologies, including retrospective medical record analysis, longitudinal patient registries, case-control investigations, and cross-sectional epidemiological studies. Our platform enables researchers to:
Generate robust real-world evidence (RWE) and real-world data (RWD) to inform clinical practice and healthcare policy decisions. The platform captures nuanced patient experiences and treatment outcomes across diverse populations and healthcare settings.
Evaluate the complex interplay between risk factors and clinical outcomes through advanced statistical modeling. This includes assessment of both modifiable and non-modifiable risk factors that influence disease progression and treatment response.
Track medication utilization patterns, therapeutic adherence rates, and treatment persistence through sophisticated data capture mechanisms. The platform enables detailed analysis of prescription patterns, dosing regimens, and patient compliance factors..
We Transform Your Vision into Creative Results
We asked 2536 researchers from different sectors about the services that they currently recieve to conduct their studies. Our results have shown that:
A significant majority of researchers, 81%, express dissatisfaction with their current EDC. Common complaints include the prohibitive cost of EDC software licenses, coupled with a failure to deliver on promised services and features. Furthermore, researchers often find themselves forced to utilize multiple software platforms to meet all their research needs, highlighting a gap in functionality within existing solutions. Chellsy addresses these challenges by offering a cost-effective, comprehensive platform that eliminates the need for multiple software subscriptions and provides the necessary tools and support for efficient and successful research.
Nearly half of all researchers, 47%, find the training process to run an EDC complex and time-consuming, often compounded by inadequate customer support. Furthermore, a majority of data mangers report that existing software lacks essential features, forcing them to constantly switch betweendifferent platforms and disrupting their workflow.
Chellsy’s efficient process can be particularly beneficial for dossier submissions, where accurate and well-managed data is essential for regulatory success.
FEATURES
Advanced Features
All in Unique Platform
STATISTICAL
ANALYSIS
- Data analyses, modelling data to understand risk, benefit and effectiveness of treatments
- Data management and cleansing
- Descriptive: frequencies, mean, SD, tables and etc.
- Analytical: modelling data (Logistic, Linear, Cox or Poisson regressions)
Chellsy offers great solutions to conduct observational studies such as retrospective chart review, patient registries, case-control and cross-sectional. Chellsy helps you on:
- Provide information on “real world” use and practice
- Detect signals about the benefits and risks of treatment or products in the general population
- Burden of disease and identification of unmet needs
- Treatment patterns, drug utilization, adherence
- The identification and impact of risk factors on disease outcomes
- Comparative effectiveness
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ABout US
Our research consulting services are led by experienced epidemiologists who bring a deep understanding of study design, data analysis, and public health principles to every project. Their expertise allows us to provide comprehensive support for a wide range of research needs, from developing robust study protocols and managing data collection to conducting advanced statistical analyses and interpreting findings. This epidemiological background ensures that our clients receive methodologically sound and scientifically rigorous research, leading to reliable and actionable results.
Medy Ehtesham
Research Consultant
Epidemiology consultant with over a decade of experience in designing and managing observational studies. Currently leading regulatory consumer research at PMI Science. Specializes in translating complex findings into actionable insights. Extensive experience across multiple therapeutic areas including COVID-19, Oncology, Cardiovascular, and Respiratory. Skilled in project management, stakeholder engagement, and regulatory submissions. Passionate about leveraging data to improve public health outcomes and inform evidence-based decision making.
Your business and your customers are our passion. Technology is our speciality.
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