CDConnectTM
Streamline your study with secure clinical trial data management software
CDConnect™ addresses the challenge of managing and unifying data from diverse sources in clinical trials by delivering cutting-edge clinical data management software with real-time data capture, essential analytics, strong security, and seamless integration with various devices and systems.
Elevate your clinical research today.
Managing clinical data in decentralized trials can be complex.
- Ensuring data accuracy, completeness, and consistency across various sites and sources is tough.
- Protecting sensitive participant data and ensuring compliance with data privacy regulations is challenging.
- Integrating research data from multiple sources, including wearables and in-home medical devices, can be demanding.
- Adhering to evolving regulatory requirements and guidelines is arduous.
CDConnect™ is a robust clinical trial data management software designed to optimize your research process.
With its advanced features and intuitive interface, you can simplify your clinical study workflow and improve your operational efficiency.
CDConnect™: Your Path to Efficient and Secure Clinical Trials
CDConnect is an advanced tool that improves the clinical data management process for decentralized trials.
① Study Startup:
Seamless Data Integration
CDConnect™ simplifies data flow by allowing you to integrate data from multiple sources into one unified, user-friendly platform, ensuring data accuracy and consistency throughout the clinical study.
For decentralized clinical trials, you would need an authorization request for consent. Once obtained, our platform would start collecting data.
② Data Collection
Automated Data Entry
With CDConnect™, you can significantly speed up your data collection process and enhance operational efficiency. Effortlessly collect and consolidate real-time participant data from wearable and in-home medical devices.
Real-time Data Monitoring
Seamlessly collect and consolidate real-time data from various sources, including wearable and in-home medical devices.
Remote electronic data collection in clinical trials enhances participant engagement and maintains data accuracy. CDConnect™ also has real-time system monitoring (RTSM) for researchers to spot any trends and deviations in the data.
Efficient Database Design:
Our clinical data management software supports decentralized clinical trials with efficient, streamlined data access.
③ Data Integrity
Our system preserves data integrity and does not manipulate the study data. CDConnect passes through the data without performing processing, cleaning, or validation.
④ Data Analysis and Reporting
Immediate Insights
CDConnect’s user-friendly interface helps you get instant real-time insights into every participant’s wellness data.
The Participant Overview screen provides a concise snapshot of each participant’s recent wellness history, visualizing data collected from wearables in clear, easy-to-understand graphs. You can explore trends and averages and delve deeper into individual metrics to identify anomalies and uncover valuable insights.
Comparison Charts
Our intuitive dashboard makes it easy to compare participant wellness metrics, identify trends, and spot anomalies across any timescale. Gain valuable clinical insights with just a few clicks.
Customizable Dashboard
Experience added flexibility with our customizable dashboards and screens.
Easily tailor your view with a few simple clicks, whether you need a comprehensive trial overview or delve into specific metrics. Our intuitive interface ensures all critical information is readily accessible, helping you gain valuable insights from your research.
⑤ Data Security and Compliance Process
Immediate Insights
Our steadfast security measures include state-of-the-art data encryption techniques, regular security audits, strict access controls, reliable data backup and recovery, and data compliance with regulatory requirements.
We make sure the data and processes are compliant with all applicable industry standards and regulatory requirements.
Leveraging CDConnect can accelerate clinical trials, improve data quality, and advance your clinical research
Uncompromising Security: Your Clinical Trial Data, Protected
CDConnect is committed to protecting your sensitive clinical data. We’ve achieved an A+ cybersecurity certification, a testament to our rigorous security standards. With CDConnect, you can have peace of mind knowing that your clinical trial data is secure.
We firmly believe that your data belongs to you. CDConnect™ does not use or share your data for any purpose other than enabling you to access, manage, and analyze it within the platform. Our system is designed to ensure that your data is solely under your control, maintaining the highest level of privacy and ethical standards.
Our Mission Is To…
“…empower researchers and data analysts by simplifying the capture, integration, and analysis of clinical trial data from wearables and in-home medical devices, enabling smarter, faster, and more reliable research outcomes.“
Let’s Shape the Future of Medical Research Together!
We call all doctors, healthcare professionals, clinical trials experts, and investors! We invite you to join our mission to revolutionize the clinical trials landscape.
We call all doctors, healthcare professionals, clinical trials experts, and investors! We invite you to join our mission to revolutionize the clinical trials landscape.
Your valuable ideas and feedback can help shape the future of CDConnect and make it better for medical and research communities.
We’re passionate about fostering a collaborative environment and making a meaningful impact on clinical trial management. We’re eager to hear from you, learn about your experiences, and understand how we can better serve your needs.
Let’s work together to shape the future of medical research!
Ready to transform your clinical research operations?
Handle your clinical trial data more efficiently.
Yes to a faster and more accurate data management system.
Collaborate with us and start optimizing your clinical trial process.
Frequently Asked Questions
Clinical trial data management is a part of clinical trial management that is concerned with collecting, cleaning, and managing data from clinical trials. It involves ensuring the accuracy, completeness, and consistency of data collected throughout the trial. This process is crucial for generating reliable results and making informed decisions about drug development and medical treatments.
Clinical data management emerged as a response to the pharmaceutical industry’s need for rigorous and reproducible research. To ensure data integrity and compliance with regulatory standards, drug companies adopted structured approaches to data collection, analysis, and reporting. This evolution has led to the widespread use of software-based systems that streamline data management, enhance data quality, and speed up clinical trial timelines.
CDConnect™ is ideal for clinical research organizations (CROs), pharmaceutical companies, academic institutions, and medical device manufacturers conducting clinical trials, especially decentralized or hybrid studies.
Yes, CDConnect™ integrates seamlessly with wearable devices and in-home medical devices, allowing for a comprehensive and unified data collection process.
Absolutely. CDConnect™ ensures compliance with evolving regulatory requirements, including GCP, ICH, FDA guidelines, and other regional standards, streamlining audit readiness and regulatory submissions.
Yes, CDConnect™ is committed to safeguarding your clinical trial data.
We take data security seriously, so we partner with a leading cybersecurity firm to conduct regular audits, ensuring the highest level of protection for your study data. Our clinical research data management software has achieved an A+ cybersecurity certification, reflecting our commitment to industry-best practices.
To further safeguard your research data, we leverage Amazon Web Services (AWS) in our cloud-based system and implement robust security measures. Our cloud-based solutions prioritize confidentiality by assigning unique participant IDs, eliminating the need for additional personal information.
CDConnect™ is designed for ease of implementation with intuitive onboarding, dedicated support, and integration capabilities to align seamlessly with existing systems and processes, even in ongoing trials.
Yes, CDConnect™ is specifically designed to support decentralized and hybrid clinical trials. Its capabilities include remote data collection, seamless integration with patient devices, and tools to enhance patient engagement and trial oversight.
Yes, CDConnect™ is scalable and optimized for managing multi-site clinical trials. Its robust features ensure consistent data quality and compliance across all trial locations.
Yes, at CDConnect™, we prioritize the confidentiality and security of your clinical trial data.
To ensure the highest level of security, we partner with a highly reputable third-party cybersecurity firm to conduct rigorous audits of our systems. Our platform has earned an A+ cybersecurity certification, reflecting our commitment to safeguarding your data with industry-leading standards and practices.
We leverage Amazon Web Services (AWS) and implement robust data security measures to safeguard your information. Confidentiality and blinding are maintained by assigning unique participant IDs during registration. No additional personal information is required to start collecting data.
CDConnect™ enhances participant engagement by offering flexible, remote monitoring and easy-to-use tools that simplify data collection processes. The platform empowers participants with virtual trial capabilities, ensuring their involvement without adding unnecessary burdens. This efficient approach not only improves engagement but also supports better compliance with trial protocols.
Yes, CDConnect™ is designed to reduce the operational burden of managing decentralized and hybrid clinical trials. By centralizing trial activities and integrating real-time data monitoring and analysis, the platform streamlines workflows, simplifies trial oversight, and accelerates decision-making processes, enabling sponsors and research teams to focus on trial outcomes.