About Cisiv ltd
Cisiv Ltd: Revolutionizing Real World Studies with Cutting-Edge Technology
Cisiv Ltd is a leading provider of technology solutions for real world studies. Established for 15 years, the company has built a reputation for excellence in the industry, thanks to its innovative approach and commitment to delivering results that exceed expectations.
At Cisiv, we understand that conducting real world studies can be challenging. There are many variables to consider, from patient recruitment and data collection to analysis and reporting. That's why we have developed a suite of tools and services that streamline the process, making it easier for our clients to achieve their goals.
Our core technology is designed specifically for phase IV studies, which are conducted after a drug or medical device has been approved by regulatory authorities. These studies aim to gather additional information about the safety and effectiveness of the product in real-world settings. They are critical for ensuring patient safety and informing clinical practice.
At Cisiv, we recognize that every study is unique. That's why we work closely with our clients to understand their specific needs and develop customized solutions that meet those needs. Our team of experts includes statisticians, programmers, project managers, data managers, medical writers and regulatory specialists who work together seamlessly to deliver high-quality results on time.
One of our key strengths is our ability to adapt quickly as new technologies emerge or regulations change. We stay up-to-date with industry trends so that we can offer cutting-edge solutions that give our clients a competitive edge.
Our suite of tools includes:
1) EDC (Electronic Data Capture) - Our EDC system allows researchers to collect data electronically from study participants using web-based forms or mobile devices.
2) IWRS (Interactive Web Response System) - Our IWRS system enables randomization of patients into different treatment groups while ensuring blinding.
3) CTMS (Clinical Trial Management System) - Our CTMS system provides centralized management of all aspects of a clinical trial, including study timelines, budgets, and resources.
4) Data Analytics - Our data analytics team uses advanced statistical methods to analyze study data and provide insights that inform decision-making.
In addition to our technology solutions, we also offer a range of services to support real world studies. These include:
1) Study Design - We work with clients to design studies that are scientifically rigorous and meet regulatory requirements.
2) Project Management - Our project managers ensure that studies are delivered on time and within budget.
3) Medical Writing - Our medical writers produce high-quality documents such as protocols, clinical study reports (CSRs), and manuscripts for publication in peer-reviewed journals.
4) Regulatory Support - We provide regulatory support throughout the study lifecycle, from protocol development through submission of final reports.
At Cisiv Ltd, we are committed to delivering results that exceed expectations. Our focus on innovation, quality and customer service has earned us a reputation as a trusted partner for real world studies. Contact us today to learn more about how we can help you achieve your goals.
cisiv.com
