Medicai’s cloud-based PACS seamlessly integrates with any CTMS to organize medical imaging data, enabling real-time data flow across multiple trial sites. Our solution offers advanced security, granular access control, de-identification and re-identification, and AI integration, ensuring strict compliance. Streamline retrieval, viewing, storage, and sharing without installations or local downloads.
Medicai provides a cloud-based PACS and DICOM viewer solution that seamlessly integrates with any CTMS, ensuring centralized and real-time access to imaging data. With automated data capture, advanced analytics, and AI-driven insights, Medicai significantly enhances data consistency, accelerates clinical trial workflows, and improves patient management.
Our platform guarantees strict regulatory compliance, maintaining detailed audit trails and secure data storage for HIPAA, GDPR, and FDA standards. Through streamlined collaboration tools, annotation features, and customizable dashboards, research teams can make informed decisions quickly.
By reducing manual processes and optimizing resources, Medicai’s imaging services for clinical trials drives efficiency, shortens trial timelines, and supports faster drug development.
Some of the key features of our imaging solution for CTMSs are:
Since Medicai is entirely cloud-based, no software needs to be downloaded or installed for viewing any study or research. This guarantees convenience and adaptability for users taking part in clinical trial management.
Our platform complies with strict privacy laws and regulations regarding clinical software solutions, ensuring the security of the system and the privacy of sensitive medical imaging data.
Integrated checks and audit logging features help users adhere to regulatory requirements throughout the clinical trial process.
Role-based access control ensures that only authorized personnel access specific medical imaging data, enhancing security and privacy.
Medicai provides safe, long-term DICOM storage, guaranteeing data availability and integrity during clinical studies.
We have protocols for anonymizing patient information. Pharma companies are not allowed to interact with the protected health information of patients. Other providers might also face restrictions on their ability to interact with PHIs. Therefore, Medicai's de-identification engine enables them to establish automated workflows.
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Medicai’s Clinical Trials PACS software transforms trial management with seamless imaging integration, real-time data access, and advanced analytics. Enhance compliance, streamline workflows, and accelerate timelines while reducing costs.
Medicai’s cloud-based platform ensures instant, secure access to medical images, enabling researchers and clinicians to collaborate from any location. Real-time synchronization means updated data is always available, drastically reducing lag times. This on-demand accessibility accelerates trial workflows, allowing for faster decision-making and ultimately boosting the overall quality of research outcomes.
By seamlessly integrating PACS with your CTMS, Medicai eliminates manual data entry errors and ensures consistent imaging data across all trial sites. Automated processes, combined with secure data capture methods, maintain high-quality data integrity. This level of precision leads to more reliable outcomes and offers dependable support for regulatory submissions.
Medicai is designed to meet stringent standards, including HIPAA, GDPR, and FDA regulations, ensuring compliance throughout your clinical trial’s imaging workflow. Our system automatically logs audit trails for every image interaction, maintaining transparency and accountability. This robust compliance framework significantly mitigates risk and accelerates the approval process for treatments.
Medicai supports annotation, sharing, and messaging features directly within the PACS environment, uniting geographically dispersed research teams. This collaborative approach allows for rapid feedback on imaging findings, eliminating communication gaps. By fostering real-time dialogue, Medicai helps your team make quicker, evidence-based decisions that keep trials on schedule and under budget.
By integrating imaging data management within your existing CTMS, Medicai reduces duplication of tasks and lowers operational overhead. Automated processes and robust analytics help identify inefficiencies and streamline resource allocation. This efficient approach ultimately cuts costs, conserves staff time, and delivers faster results without compromising quality or patient safety.
Medicai integrates with AI and machine learning algorithms to automate image analysis, revealing critical patterns and predicting outcomes sooner. These intelligent tools highlight anomalies, quantify disease progression, and even suggest optimal treatment pathways. This level of insight empowers faster, evidence-based decisions, expediting trial timelines and enhancing overall research reliability.
Medicai's platform provides an intuitive user interface for uploading, storing, and exchanging medical images for clinical trials. There is no need for complex software installations because users can safely access the platform from any device with an internet connection. Throughout the clinical trial process, role-based access control and built-in compliance checks guarantee that sensitive data is compliant and safe.
Due to its interoperability, Medicai can be integrated with any other clinical trial platform or clinical trial automation software. Also, we can connect multiple clinical research sites, making them work as one.
Our multi-enterprise solution enables a new approach to clinical trials. Connect and retreive imaging studies for patients enrolled in the clinical trials directly from the participating centers.
Medicai's interoperable imaging infrastructure provides a robust foundation for multi-location clinical trials. The infrastructure can store studies, together with other medical documents and files (including pathology studies), in a secure and compliant way.
Our imaging orchestration layer enables automatic connections with AI companies and manages the processes of de-identification and re-identification.
Access control is granular and easy to define and manage.
Clinical trial data can be accessed and visualized through our web portal and mobile apps. Both frontends embed the DICOM Viewer.
The Medicai accounts are multi-organization, so if a doctor or a researcher participates in multiple clinical trials, they can view the data from the same user account.
Collaboration is easy with Medicai's functionality: audio/video calling, messaging, notifications, and document signing.
Pharma companies have access to aggregated, anonymized (de-identified) data and can easily manage the progress in real time.
Imaging and DICOM capabilities can be embedded in already-existing clinical trial management software using our APIs.
Give it a try, play with it! Using our embeddable DICOM Viewer, you can easily view your DICOM files anywhere online (web, in the mobile application). Your DICOM files are stored in your Medicai workspace, in your cloud PACS.
With Medicai, we can access patient medical data like CT scans and other medical documents. We organize our multidisciplinary discussions of diffuse interstitial lung diseases online, using the Medicai platform. These discussions aim to establish a definite diagnosis and bring consensus on the therapeutic recommendations.
MD. PhD. Claudia Toma
,
Senior Lecturer and Expert Pulmonologist with IPF/ILDs
@
"Carol Dávila" University of Medicine and Pharmacy
Choose Medicai as your trusted clinical trials imaging company and experience unrivaled data accessibility, streamlined workflows, and robust compliance. As a top-tier imaging vendor for clinical trials, we excel in the dynamic diagnostic imaging clinical trials market, offering real-time collaboration, AI-driven insights, and transparent audit trails. Empower your research with faster, better-informed decisions—partner with Medicai today for results.
What should be considered when choosing a cloud PACS with DICOM viewer for clinical trials?
When selecting a cloud PACS with a DICOM viewer for clinical trials, consider factors such as compatibility with existing clinical trial management systems, the scalability to handle large volumes of data, and the availability of advanced imaging tools and functionalities. It's also important to evaluate the vendor's support services, the system's uptime guarantees, and how well the system integrates with other data management and analytical software used in clinical trials.
How does a cloud PACS with DICOM viewer contribute to regulatory compliance in clinical trials?
A cloud PACS with a DICOM viewer helps ensure regulatory compliance by providing robust data encryption, secure user access controls, and comprehensive audit trails that record every interaction with the data. This technology supports adherence to HIPAA in the U.S., GDPR in Europe, and other regional data protection regulations, which is critical for global clinical trials. Additionally, it facilitates the anonymization and pseudonymization of patient images, crucial for protecting patient privacy.
What advantages does integrating a cloud PACS with DICOM viewer provide in clinical trials?
Integrating a cloud PACS with the DICOM viewer in clinical trials allows for enhanced data accessibility and collaboration. This setup supports real-time data sharing among geographically dispersed research teams and trial sites, facilitates secure storage and management of medical images, and ensures compliance with health data regulations. Furthermore, it improves image analysis efficiency and helps to maintain high data integrity and reproducibility of results.
What systems are used in clinical trials?
In clinical trials, essential components include Electronic Data Capture Systems (EDC's), Patient Databases, Biostatistics Software, and Regulatory Compliance Tools, with Medical imaging management Systems playing a critical role in the efficient handling and analysis of imaging data.
Seamlessly retrieve, view, store, and share medical imaging data with a robust multi-location, cloud PACS storage, zero-footprint DICOM viewers, AI support, and best-in-class sharing capabilities.
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