We focus on data capture, statistical analysis, and clinical trial reporting
Our primary focus is on data capture, statistical analysis, and clinical trial reporting. Leveraging our expertise in clinical data management, we swiftly assemble high-quality teams that provide flexible and tailored solutions to meet the unique demands of each clinical study. With a commitment to delivering exceptional outcomes, we ensure that our services address every phase of the clinical trial process.
We offer a range of specialized services, including Clinical Data Management, where we ensure the accurate, timely, and efficient collection and organization of data throughout the trial lifecycle. Our Biostatisticsservices support the design, analysis, and interpretation of clinical data, helping researchers make informed decisions backed by robust statistical evidence. Through Statistical Programming, we develop complex, reliable programs to handle and analyze large datasets with precision and reproducibility, ensuring consistency across trials.
Furthermore, our Statistical Consultancy service provides strategic guidance on study design and statistical methodologies, ensuring that every clinical decision is backed by sound, evidence-based statistical reasoning. We also specialize in Statistical Methodology Research, advancing new techniques and approaches in statistical analysis to solve complex challenges in clinical trials. This expertise allows us to offer cutting-edge solutions that enhance the reliability and efficiency of trial outcomes.
By integrating these services, we deliver comprehensive, high-quality solutions that meet the evolving needs of clinical trials, ensuring success at every stage of the process.
Our History
Founded with a vision to revolutionize clinical research, our company began as a small team of experts driven by a passion for data science and healthcare innovation. From the outset, we recognized the growing need for accurate, efficient, and compliant data management in clinical trials, and we set out to build a company that could meet this challenge head-on.
Our Mission
Our mission is to advance healthcare and improve patient outcomes by delivering innovative, data-driven solutions for clinical research and trials. We are committed to providing exceptional quality in data management, statistical analysis, and regulatory reporting, ensuring that every clinical study is conducted with the highest level of accuracy, integrity, and compliance.
Who We Are
Our primary focus is on data capture, statistical analysis, and clinical trial reporting. We swiftly assemble high-quality teams that provide flexible and tailored solutions to meet the unique demands of each clinical study. With a commitment to delivering exceptional outcomes, we ensure that our services address every phase of the clinical trial process.
Why Choose Veliki?
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Easy to Deploy
Easy to Deploy
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Cost Effective
Cost Effective
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Simple & Flexible
Simple & Flexible
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Real-Time Alerts
Real-Time Alerts
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Massively Scalable
Massively Scalable
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Robust Security
Robust Security
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Meet The Team
Our team is a group of highly skilled professionals with expertise in clinical data management, biostatistics, pharmacovigilance, and regulatory affairs. Together, we are dedicated to delivering innovative, data-driven solutions to advance healthcare and improve patient outcomes.
Dr. Atanu Bhattacharjee
Director, Co-founder atanu@statscure.co.in
Vivek Sharma
Director, Co-founder vivek@evahworld.com
Oindrila Roy Chowdhury
Director, Co-founder, oindrila@statscure.co.in
Akash Pawar
Director, Co-founder, akash@statscure.co.ineClients Feedback
Here are twelve client feedback examples that highlight different aspects of service and performance in clinical research and data management
The team’s expertise in biostatistics was instrumental in the success of our trial. Their attention to detail ensured accurate data analysis and reporting.
Filip Luis
Founder & CEOWe appreciate the flexibility and responsiveness of the team. They tailored their approach to meet our specific needs, making the entire process seamless.
David Luiz
DesginerThe quality of the medical writing exceeded our expectations. Every document was clear, comprehensive, and compliant with regulatory standards.
Sarah Taylor
ManagerThanks to their effective risk management strategies, we were able to navigate potential challenges quickly and efficiently, keeping our trial on track.
James Anderson
DeveloperThe real-time data monitoring provided by the team allowed us to make informed decisions that enhanced patient safety and trial integrity.
Their innovative use of big data analytics significantly improved our patient recruitment process, leading to faster enrollment and reduced costs.
The pharmacovigilance services were top-notch. We felt confident that patient safety was the team’s top priority throughout the trial.
Their commitment to excellence was evident in every interaction. We felt supported and well-informed at each stage of our project.
The operational efficiency of their team is impressive. They streamlined our processes, resulting in a quicker turnaround time for our study.
Their statistical consultancy provided invaluable insights that enhanced our study design, ultimately leading to more robust outcomes.
The collaborative approach they took fostered a strong partnership, making it easy to communicate and resolve any issues that arose.
We were particularly impressed with their ability to adapt to changing regulatory requirements, ensuring compliance without disrupting our timeline.
Big Data Value & Benefits
Big data has revolutionized the landscape of clinical research and healthcare, offering unprecedented value and a host of benefits that drive better decision-making, faster drug development, and improved patient outcomes. By harnessing vast amounts of data from diverse sources, including electronic health records (EHRs), clinical trials, wearable devices, and genomic data, big data provides a deeper and more comprehensive understanding of disease patterns, treatment responses, and patient populations.
Risk Management
Risk management in clinical research and healthcare is the process of identifying, assessing, and mitigating potential risks that could affect the success of clinical trials or patient safety. It involves proactive planning to minimize adverse events, ensure data integrity, and maintain compliance with regulatory standards. Key components include continuous monitoring of trial progress, assessing safety signals, and applying corrective actions as needed.
Effective risk management enhances decision-making, reduces the likelihood of trial delays, and safeguards patient well-being. It also ensures that trials are conducted ethically and efficiently, with a focus on both scientific validity and patient safety. By systematically addressing risks, organizations can avoid costly setbacks and maintain trust with stakeholders.
Operations Management
Operations management in clinical research and healthcare involves overseeing the day-to-day activities that ensure clinical trials and healthcare services run smoothly and efficiently. It encompasses the planning, coordination, and execution of various processes, from patient recruitment and data collection to resource allocation and regulatory compliance. The goal is to optimize workflows, minimize delays, and ensure that trials meet their objectives on time and within budget.
Key aspects of operations management include project planning, supply chain management, quality control, and risk management. It also involves the coordination of cross-functional teams, ensuring that all stakeholders—clinical staff, data managers, statisticians, and regulatory experts—work in sync to achieve trial goals.
By streamlining operations and maintaining high standards of efficiency and quality, operations management helps improve trial outcomes, reduce costs, and accelerate the development of new therapies while ensuring patient safety and data accuracy.
Unlock the potential of medical data with StatsCure. Our advanced analytics solutions empower healthcare providers to make informed decisions, enhance patient outcomes, and streamline operations, driving a new era of efficiency and precision in healthcare. (Below the log bottom left)
Sample Size Estimation: Ensuring the Success of Your Clinical Trials
Sample size estimation is a crucial step in designing effective clinical trials, guaranteeing that studies have sufficient statistical power to detect true effects. Our expertise in this area ensures that you can confidently navigate the complexities of trial design. By accurately calculating the minimum number of participants required, we help you balance resource constraints with the need for robust findings.
- Accurate determination of participant needs
- Optimal balance between resource allocation and reliability
- Enhance the credibility of your study results
The process begins by defining your study’s primary endpoint and anticipated effect size. We leverage previous studies, pilot data, and expert insights to provide precise estimates tailored to your specific research goals. Understanding variability in outcome measures is essential, as it directly influences the necessary sample size. Our team will guide you through selecting the appropriate significance level and power, ensuring a comprehensive approach to your trial design.
- Customized estimates based on your research goals
- Insightful analysis of outcome variability
- Expertise in significance level and power selection
Utilizing advanced statistical formulas and software tools, we facilitate sample size calculations tailored to your study design, whether it’s a parallel, crossover, or cluster randomized trial. Our biostatistical experts are on hand to assist you in making valid assumptions and conducting sensitivity analyses to assess how variations impact your sample size requirements.
- Advanced statistical tools for precise calculations
- Expert support throughout the planning process
- Sensitivity analyses for robust study design
Ultimately, effective sample size estimation enhances the integrity and reliability of your clinical trials. By ensuring studies are adequately powered, we empower you to draw meaningful conclusions that advance medical knowledge and evidence-based practices. Trust us to help you minimize unnecessary risks for participants while maximizing the impact of your research.
- Improved reliability and validity of trial outcomes
- Ethical conduct through responsible participant exposure
- Contributions to the advancement of medical research