5 Must-Haves While Choosing the an EDC Platform for Your Next Trial
Recent Articles Simplifying eCRFs: A Look at the Future of Clinical Data Management July 8, 2024 Read More AI-Powered Clinical Data Validation: Ensuring Accuracy, Efficiency, and Compliance September 21, 2024 Read More AI in Clinical Trials: Key to Accelerated Timelines & Reduced Costs July 29, 2024 Read More 5 Must-Haves While Choosing the an EDC Platform for Your Next Trial Manuj Vangipurapu / Jan 29, 2024 As 2023 wrapped up, clinical research is on the cusp of an exciting new era. AI-powered data analysis, and real-time data are transforming the way we conduct studies. To stay ahead of the curve, choosing the right Electronic Data Capture (EDC) platform is more crucial than ever. But with a plethora of options available, what should be your top priorities while choosing an EDC? 5 Must-Haves for Your Next EDC Platform: The below list consists of features which a new age EDC must have coupled with specific features. 1. Leverage the Power of AI: Auto-Pilot Tasks, Unleash Insights Artificial intelligence is now part and parcel of the clinical trial. EDC software infused with AI can revolutionize your trials by: Automated Study setup: From protocol design to case report form creation and CDASH coding; AI enables automated study setup and reduced build timelines Proactive query management: Identify and flag potential data inconsistencies in real-time, preventing delays and ensuring data quality. Predictive risk assessment: Leverage AI to predict potential safety issues or study setbacks, enabling proactive interventions. 2. Ease of Use: Built for You, Not Tech Geeks Forget cryptic interfaces and endless training days. Your EDC should be as intuitive as your smartphone, built for researchers, not programmers. No more steep learning curves and integration headaches, just streamlined workflows and accelerated study progress. Intuitive interface: Automated builds with in-built standards, intuitive navigation and minimal errors during data entry. Role-based access and permissions: Tailored interfaces for different user roles (CRCs, investigators, etc.) to ensure data security and efficient workflows. Days instead of weeks building CRFs: Choose a system with a standardized Global Library that lets you build forms in days, not weeks. 3. Unified Platform: Breaking Down Data Silos, Fostering Collaboration Modern EDC platform provides end to end solutions, real-time dashboards and visualizations, allowing you to work across multiple applications seamlessly, aggregating information and providing a centralized interface for complete study oversight. Embrace ePRO and CTMS Integration: Seek an EDC platform that seamlessly integrates with ePRO and CTMS, eliminating data silos and streamlining workflows. Standardized Data Formats: Ensure the platform supports relevant data formats like DICOM, HL7, and CDISC to facilitate data exchange with other systems. Regulatory Compliance: Look for an EDC platform with specific validation for studies, following regulations like FDA 21 CFR Part 11, EU MDR/IVDR, and ISO 13485. Look for an EDC equipped with advanced features like data loaders, custom reporting tools, and comprehensive analytics. Advanced reports and visualization: Drill down into your data with powerful reports, interactive charts, and graphs to uncover hidden patterns and trends. Data security and compliance: Choose an EDC system with robust security features and adherence to relevant data privacy regulations like GDPR and FDA 21 CFR Part 11. Maximize Value, Not Costs: Choose an EDC platform that includes features like AI-enabled CDASH mapper, rSDV automation, Data Loader, AI Medical Coding and advanced dashboards as a standard. 5. Value for Money: Maximize Efficiency, Minimize Costs Research budgets are precious, so choose an Electronic Data Capture (EDC) platform that delivers real value at every turn. Ditch outdated tools that drain resources and drag down productivity. Choose an EDC that works in tandem with you, maximizing efficiency and minimizing cost while delivering deeper insights. Invest in efficiency, unlock savings: Powerful automation features, faster study setup, AI-powered tools, and streamlined processes deliver significant cost efficiencies – all at the cost of a traditional EDC. Flexible pricing models: Choose a platform that aligns with your budget. Look for flexible pricing models and options that cater to your specific study needs and duration. Don’t get stuck with pre-built reports: Choose a system that allows you to customize reports and delve deeper into device-specific data, gaining actionable insights for informed decision-making. Remember, the right EDC platform is an investment in the future of your clinical trials. By carefully considering these trends and often-overlooked factors, you can choose a solution that empowers your research, protects your data, and sets you up for success in 2024 and beyond. See How our Clinion EDC can empower your 2024 trials and beyond! Contact Us
Top 5 Reasons to Choose Clinion’s AI-Enabled eClinical Platform for your next trial
Recent Articles Simplifying eCRFs: A Look at the Future of Clinical Data Management July 8, 2024 Read More AI-Powered Clinical Data Validation: Ensuring Accuracy, Efficiency, and Compliance September 21, 2024 Read More AI in Clinical Trials: Key to Accelerated Timelines & Reduced Costs July 29, 2024 Read More Top 5 Reasons to Choose Clinion’s AI-Enabled eClinical Platform for your next trial Manuj Vangipurapu / November 20 2023 Choosing the right eClinical vendor is the cornerstone of successful trials. An inadequate choice can lead to a cascade of challenges, from data inaccuracies to operational inefficiencies. In this complex landscape, Clinion isn’t just a platform – it’s a seasoned guide adeptly navigating clinical trials with transparency, precision, and an innate understanding of the challenges. Now, let’s break down the core reasons why Clinion is the linchpin for your clinical trial success. Reason 1: User-Centric All the Way Clinion’s platform is designed with you in mind. From trial inception to completion, our eClinical platform prioritizes user needs, ensuring a seamless and user-friendly journey. The system is built to be accessible and relevant to the specific needs of different users. We prioritize user-friendly interactions to enhance efficiency and reduce the learning curve for all stakeholders. By providing role-specific dashboards and features like global libraries , we ensure that each user maximizes trial efficiencies without unnecessary complexities. Clinion strives for simplicity and speed. By actively incorporating user feedback, we ensure continual refinement for optimal efficiency. Reason 2: Supports Complex Trials Supporting the diverse landscape of clinical trials requires a platform that can adapt and evolve. Clinion empowers researchers to handle the complexities of modern clinical trials with ease. Whether it’s a simple trial or a highly complex study ( DCT, hybrid , or any therapeutic area) our platform adapts seamlessly, providing robust functionality for every type of clinical research. Clinion’s scalability allows for smooth integration of modules, adapting effortlessly to the intricacies of your research, be it a single-site trial or a complex multi-arm study. Our systems are put to test in countless clinical trials, ensuring your data and processes remain resilient and dependable. The safety and integrity of data are guaranteed , with compliance to regulatory standards such as ISO 9001, ISO 27001, GDPR, and ICH GCP. Reason 3: A Unified Solution for Every Trial Need Clinion stands as a unified solution catering to the diverse needs of clinical trials. This holistic approach ensures a seamless and integrated experience, addressing every aspect of trial management with a unified strategy. Platform is integrated ensuring cohesion across every phase, eliminating the hassle of juggling multiple systems. Minimizes data silos, reduces manual work, by creating a unified hub for all your trial needs. Access central lab data, EDC, and data from external sources, including ePRO, within a single system in the fastest and most reliable manner. Reason 4: Future-Proof Clinical Trials With AI Clinion propels clinical trials into the future with the integration of Artificial Intelligence (AI). This forward-thinking approach enhances efficiency, accuracy, and overall trial success by harnessing the power of cutting-edge AI technology. AI medical coding swiftly assigns accurate codes based on provided terms, reducing coding time by 70%-80% compared to interactive coding. CSR Automation helps you generate 70% of the report allowing for faster submissions. eProtocol reduces protocol design times and disruptions by providing optimal protocols from the knowledge base, minimizing amendments. Automated Source Data Verification (SDV), which systematically checks and validates trial data, guaranteeing accuracy and efficiency in a blink. Reason 5: Optimized Cost of Ownership Clinion doesn’t just streamline clinical trials; it significantly reduces the cost of ownership. Our platform is engineered to optimize resource utilization, enhance operational efficiency, and ultimately minimize the financial footprint of managing clinical trials. We offer a flat per study per month pricing model that facilitates transparency and fairness. Clinion offers AI capabilities at the cost of traditional systems giving unparalleled value for your investment. Enhance your system with value-added features like data loader and AI medical coding at no extra cost. Conclusion In conclusion , clinion emerges as a solution adept at addressing the data challenges faced by clinical trial professionals. By enhancing the collaboration and management of sensitive data among sites, contract research organizations, sponsors, and trial participants, clinion proves to be a valuable ally in ensuring a smooth and streamlined experience throughout the trial process. The best way to truly grasp the Clinion advantage is to experience it firsthand Dive into our demo and let the platform speak for itself Contact Us
The Evolution of Generative AI: Capabilities, Future and Implications for Clinical Research
Recent Articles AI-Powered Clinical Data Validation: Ensuring Accuracy, Efficiency, and Compliance September 21, 2024 Read More AI in Clinical Trials: Key to Accelerated Timelines & Reduced Costs July 29, 2024 Read More Simplifying eCRFs: A Look at the Future of Clinical Data Management July 8, 2024 Read More The Evolution of Generative AI: Capabilities, Future and Implications for Clinical Research Vijay Bhaskar Reddy Velagala / Oct 03 2023 Introduction In the early years, your phone’s predictive text made you wonder, then came Gmail’s Smart Reply feature that utilizes machine learning to provide one-sentence responses. Since then we have come a long way, all thanks to Generative AI or GenAI. This technology is now capable of creating art, composing coherent paragraphs, writing code, and even assisting scientists in clinical research. But what exactly is Generative AI, how has it evolved, and what role can it play in clinical research? Let’s delve deeper! What is Generative AI? Generative AI, in simple terms, is a type of artificial intelligence that can create things on its own, like writing text, generating images, or even composing music. It’s like having a computer program that can come up with new ideas and create content without human input. Generative AI learns from existing data and uses that knowledge to generate new and creative content, making it useful in various fields, from writing stories to designing artwork. The Evolution of Generative AI The Early Days The initial forms of generative AI were very basic. It could barely suggest some random words and generate single sentences based on traditional machine learning algorithms which were not very useful. The main challenge was to make these systems ‘learn’ like a human does. Examples are the phone text and Gmail. Deep Learning and Neural Networks The innovation in AI has advanced rapidly with the advent of deep learning and neural networks, which mimic the human brain’s structure and functions. This allowed AI models to ‘learn’ from data much more efficiently. GPT and Beyond Fast-forward to today, and we have mind-bogglingly advanced models like GPT (Generative Pre-trained Transformer). These models can write articles, hold a conversation, keep contextual understanding, provide multilingual support and even undertake logical reasoning. Capabilities So, what can modern Generative AI do? Content Creation: Write articles, and stories, or even generate artwork. Data Simulation: Generate realistic datasets for testing. Language Translation: Translate languages with high accuracy. Write Code: It can write new code, optimize the existing code, and debug code. Create Data Visualizations: Helps in creating the visualizations for the given dataset. The Future Ahead As promising as Generative AI is, it remains in its infancy, and we’ve barely scratched the surface. It’s very similar to exploring the capabilities of the human brain; we have yet to discover its full potential. Unlocking meaningful and consistent responses from Generative AI requires asking the right questions or providing the proper prompts. Organizations worldwide are recognizing the importance of Generative AI and the pivotal role of prompt engineers. These specialized individuals possess the necessary skills to interact with AI effectively, ensuring relevant and accurate responses. With this exciting landscape in mind, let’s contemplate what the future holds: Ethical Considerations: As AI gets better at generating content, questions about misinformation and data privacy will become more crucial. Collaboration with Humans: AI will work alongside humans to create even more sophisticated content. Adaptability: Future AI will adapt to individual user needs more efficiently. Generative AI in Clinical Research Generative AI holds the potential to revolutionize the healthcare industry, especially in the realms of clinical research and trials. Some areas where it can make a significant impact include: Conclusion Generative AI has come a long way from its humble beginnings. With its ever-expanding capabilities, it promises a future where machines can aid human creativity and problem-solving in unprecedented ways. The potential AI applications in clinical research and trials are particularly exciting, promising faster, more efficient, and more ethical healthcare solutions.
Clinion Earns Top Honors in the Fall 2023 G2 Ratings
Recent Articles AI-Powered Clinical Data Validation: Ensuring Accuracy, Efficiency, and Compliance September 21, 2024 Read More AI in Clinical Trials: Key to Accelerated Timelines & Reduced Costs July 29, 2024 Read More Simplifying eCRFs: A Look at the Future of Clinical Data Management July 8, 2024 Read More Clinion Earns Top Honors in the Fall 2023 G2 Ratings Vijay Bhaskar Reddy Velagala / Oct 03 2023 We are thrilled to share that Clinion has earned multiple prestigious G2 badges in the Fall 2023 G2 ratings. These badges validate our position as leaders in the Electronic Data Capture (EDC) category, reinforcing our commitment to providing efficient clinical data management solutions.
Accelerate Your Clinical Trials with Clinion EDC: Unleashing the Power of AI & Automation
Recent Articles AI-Powered Clinical Data Validation: Ensuring Accuracy, Efficiency, and Compliance September 21, 2024 Read More AI in Clinical Trials: Key to Accelerated Timelines & Reduced Costs July 29, 2024 Read More Simplifying eCRFs: A Look at the Future of Clinical Data Management July 8, 2024 Read More Accelerate Your Clinical Trials with Clinion EDC: Unleashing the Power of AI & Automation Vijay Bhaskar Reddy Velagala / Oct 03 2023 Electronic Data Capture (EDC) software has revolutionized clinical trials, enabling clinical research teams to streamline data management and enhance operational efficiency. However, the true potential of EDC is realized when coupled with advanced features that leverage AI and machine learning (ML). Among the sea of options, Clinion EDC stands out as a game-changer. Discover how Clinion EDC’s advanced AI-enabled features like eProtocol Automation, Global Libraries, AI Medical Coding and Remote SDV Automation set it apart from the competition, making it the ideal choice for accelerating your trials. eProtocol Automation – Accelerating Protocol Design and Execution Complementing its existing EDC capabilities, Clinion brings eProtocol Automation, enabling CROs and pharma companies to streamline protocol design and execution. This feature revolutionizes the creation, modification, and deployment of protocols, offering an intuitive interface and AI-driven suggestions. Users can generate the entire Protocol for a study in 3 quick steps: Users need to just upload the Protocol Synopsis to Clinion’s eProtocol Automation tool for it to generate the entire Protocol.Users can then review the Protocol and make changes as requiredUser can then commit the finalized eProtocol to the database. Weeks of effort and coordination can be reduced to a few days. Clinion utilizes the power of Generative AI to make this possible. Global Libraries – Standardization and Harmonization Made Easy Global Libraries in Clinion act as a centralized repository for study-specific data elements, forms, and even entire study designs. By leveraging Global Libraries, CROs can achieve consistent data collection and harmonization across multiple trials and sites. A study can be set up in a matter of days by utilizing Clinion EDC’s Global Libraries. Users can simply copy the required forms and/or pages over to a new study.The forms, edit checks and skip logic checks are simply copied over to the new study allowing users to validate the study and make it live.Users can also copy an entire study over and modify the forms and make it live! AI Medical Coding – Enhancing Efficiency and Accuracy As an add-on benefit, Clinion EDC introduces AI Medical Coding, augmenting the core EDC functionalities. This AI-powered feature automates the complex and time-consuming process of medical coding of clinical trials data, significantly reducing manual efforts while maintaining high accuracy. AI Medical Coding comes as a default in Clinion EDC, augmenting traditional auto and manual coding methods. Users can use AI Medical Coding as they would use traditional coding, without additional training or learning needs. By harnessing advanced machine learning algorithms, AI Medical Coding ensures swift and precise assignment of medical terms to collected data, empowering Clinical research teams with faster coding insights, improved data quality, and more efficient decision-making. Remote SDV Automation – Enhancing Efficiency and Compliance Clinion EDC’s rSDV Automation feature empowers Clinical research teams to automate source data verification remotely. Through AI-powered algorithms, ClinionAI identifies and verifies EDC data with source data, reducing the need for on-site visits. Site Users can redact and upload Source Documents into Clinion EDC. Clinion EDC then This innovative functionality not only saves time and resources but also enhances data quality, ensures compliance with regulatory guidelines, and enables CROs to make data-driven decisions more efficiently. Additionally, Clinion EDC offers an array of regular EDC features such as Interactive Dashboards, Custom Reports, Local Labs Integration, Version Management, eCRF Locks, and Bulk Locks, further enhancing the overall user experience and ensuring seamless trial management. Conclusion Clinion EDC, with its advanced AI-enabled features like AI Medical Coding, eProtocol Automation, Global Libraries, and Remote SDV Automation, unlocks the true potential of EDC for Clinical research teams. By seamlessly integrating these additional benefits with essential EDC functionalities, Clinion EDC System revolutionizes the way clinical trials are conducted. Moreover, Clinion’s commitment to innovation is evident as they continue to develop and introduce new AI use cases, aimed at making clinical trials even easier and more efficient. Experience the transformative power of Clinion EDC and stay at the forefront of cutting-edge advancements in the industry. Supercharge your Clinical Research with AI. Level up your Trials Today! Contact Us