Simplify Clinical Trials Can Play a Key Role
in Meeting Your RFP's Data Management Requirements
Do you have RFPs (Request for Proposals) for future clinical trials?
Allow Simplify Clinical Trials with its advanced platform for data management and visualization to be part of your team!
As research and development organizations continue to expand, Sponsors are confronted with a multitude of challenges. One of the most significant challenges is ensuring data management, accuracy, and security throughout their operations. The role of CRO involves conducting clinical trials for pharmaceutical and biotech companies. These CROs are required to handle vast amounts of research data throughout the clinical research process, from research protocol development to data collection, analysis, and reporting.
Simplify Clinical Trials' understands the Data Management challenges that Sponsors encounter and has developed a comprehensive solution to address the pain points. Our data management capabilities have been designed to meet global regulatory requirements, reduce cycle times, and improve data quality, ultimately supporting Sponsors in achieving excellence.
Our 'Data Management' and 'Data Visualization' services are complementary to each other i.e. while we use EDC to capture the data, we use data reporting software to visualize the data. The combined effect is having an improved ‘data visibility’, that will enable the Sponsor team to view the full picture of their clinical data.
Simplify Clinical Trials addresses the problems of Sponsors and provides them with the functionality, flexibility, and scalability required to undertake successful clinical trials:
1. Comprehensive data management services
At Simplify Clinical Trials, we provide end-to-end data management services. Our expertise in data management enables us to accelerate the clinical study process, reduce project timelines, and cut costs. We offer flexible engagement models that enhance the quality of the data - Clean, Consistent, Complete data is delivered to you!
2. Innovative technology solutions
Simplify Clinical Trials is committed to deploying innovative and cutting-edge technology solutions to provide Sponsors with efficient data management. Our state-of-the-art technology allows Sponsors to access the latest data, collaborate seamlessly with other stakeholders, and increase operational efficiency. Our CDA Module provides a platform for clinical data analytics in real-time, thereby enhancing the speed and quality of clinical data while ensuring GCP, CFR and HIPAA compliance.
3. Expertise and experience
Simplify Clinical Trials Data Management Team has been in the clinical trials industry for nearly two decades and possesses the knowledge, skills, and experience to provide Sponsors with an unmatched level of data management expertise. Our team of talented professionals has extensive experience in supporting clinical studies.
4. Ensuring data quality
Data management experts at Simplify Clinical Trials ensure that the data collected and analyzed by Sponsors is correct and meets scientific rigor and ethical standards. This is achieved by employing routine data verification, cleaning, and data reconciliation procedures, thereby minimizing errors, delays, and rework.
5. Clinical Data Analytics (CDA) - ‘Clean’, ‘Complete’ and ‘Consistent’ study data visualized
Clinical trials generate immense amounts of patient data, including data from EDC systems and multiple external data sources. Simplify Clinical Trials CDA module imports data from EDC and Vendors (Labs, ePRO etc.) and organizes it in a clean format. Using this data, we transform it into meaningful ‘Reports’, ‘Dashboards’ and ‘Interactive Visualizations’, that will provide you 'direct answers' with minimal clicks. Our CDA module automates the process of identifying data issues, therefore leaving us more time to focus on resolution of data issues, resulting in cleaner data.
6. Regulatory compliance
Our data management expertise ensures compliance with regulatory requirements, including 21 CFR Part 11, ICH Good Clinical Practice (GCP), and other global regulatory guidelines. We provide our clients with a GCP-compliant infrastructure that maintains data security, verification, audit trail, regulatory reporting, and other industry-standard practices.
Simplify Clinical Trials comprehensive data management capabilities are uniquely positioned to support Sponsors in overcoming the significant challenges they experience in clinical research oversight. Our solutions have been systematically developed to meet global regulations, reduce project timelines, and eliminate data quality concerns, a significant selling point about which potential clients can remain confident. Our team of experts is committed to delivering exceptional services to ensure our clients' success in every clinical trial. We are the industry leader in data management, and we are always up for the challenge.
Schedule an online meeting so that we can show you how our advanced platform can help you manage and visualize your data. Let's Meet!
Or if you'd like more information contact us at info@simplifyclinicaltrials.com
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