In today’s complex clinical research landscape, sponsors and CROs face numerous challenges that can impact study timelines, costs, and data quality. The iMednet platform offers innovative solutions to address these critical issues.
Accelerating Study Startup
One of the most pressing challenges in clinical trials is the time it takes to get studies up and running. iMednet studies can can be set-up in a matter of days, not weeks or months. Quick study start up is accomplished by features such as:
- Intelligent Build Tools make study builds easy, without additional programming and costly operational investment.
- Study on Demand allows you to replicate studies in just minutes.
- Creative Development Suite provides experienced study designers with flexibility in study design.
- Form Manager and its intuitive ‘drag and drop’ interface supports easy Case Report Form (CRF) layout, data field creation, data properties definition and embedded forms and shortcuts.
- Form Library automates storing and reuse of forms, form sections and individual questions in new studies.
- Workflow Manager streamlines set-up of patient and site-level CRF workflows.
- Role Based Security (RBS) makes it easy to configure permissions for study personnel.
These tools significantly reduce the time and resources needed for study startup, allowing research teams to begin data collection sooner.
Adapting to Complex Protocols
As trial designs become increasingly complex, flexibility is crucial. iMednet addresses this challenge through:
- Highly configurable CRFs that ensure compliance while maintaining flexibility
- The ability to easily adapt to mid-study changes without costly reprogramming
- A comprehensive suite of native modules that can be seamlessly integrated as study needs evolve
This adaptability allows research teams to implement complex study designs without sacrificing efficiency or incurring significant additional costs.
Enhancing Data Quality and Management
Data quality is paramount in clinical trials. iMednet offers several features to address this challenge:
- Form edit checks and other rules to ensure accurate data collection
- Real-time data access and comprehensive reporting tools for quick generation of required reports
- An enhanced Source Data Verification (SDV) tool with real-time functionality for more efficient monitoring
These features help maintain data integrity while streamlining the data management process.
Reducing Costs and Resource Requirements
Budget constraints are a constant concern in clinical research. iMednet helps address this by:
- Offering a cost-effective solution that doesn’t compromise on functionality
- Providing native modules that eliminate the need for costly integrations between separate systems
- Providing flexibility so you can invest solely in the features and functionalities your study requires through a flexible modular design.
- Enabling study teams to quickly and easily build and manage studies themselves, reducing reliance on expensive programming resources
This approach helps organizations of all sizes conduct high-quality research without breaking the bank.
Supporting Diverse Study Types
The shift towards hybrid and decentralized trials presents new challenges. iMednet is designed to support various study types by:
- Offering a flexible platform that can adapt to traditional, hybrid, and decentralized trial designs
- Providing native ePRO and eConsent capabilities and easy integration with other external data sources
- Enabling seamless data sharing through its Data Import Manager and API capabilities
This versatility ensures that research teams can meet the evolving demands of modern clinical trials.
By addressing these key industry challenges, iMednet is positioning itself as a comprehensive solution for the complex world of clinical research. Its combination of flexibility, efficiency, and robust functionality empowers research teams to conduct trials more effectively in an increasingly demanding environment.