Overview
Background
The clinical study setup process, including electronic clinical outcomes assessments (eCOA), is resource-intensive and heavily reliant on specialized skills. Challenges such as translating protocols, retrieving requirements, managing questionnaires, and generating test data are often handled manually, leading to inefficiencies and increased operational costs. Building each study from scratch is time-consuming, requiring significant resources and delaying delivery. Errors, protocol amendments, and the resulting rework further escalate costs and extend study timelines, while the lack of standardization across independently built studies results in inconsistent workflows and reduced efficiency.
Replicating successful study designs is difficult due to manual and ad hoc configurations and scaling them across multiple studies or sites requires extensive duplication of effort. Frequent protocol amendments add to the complexity, as updating the study build to reflect changes is labor-intensive and error-prone, particularly when changes impact multiple components. Additionally, extracting relevant insights from detailed protocols is challenging, leading to delays and missed opportunities to optimize trial success.
These inefficiencies directly impact data availability for sponsors, CROs, and regulatory authorities, slowing decision-making and increasing time-to-market. The manual nature of the setup also makes onboarding new team members time-consuming, as they must learn intricate processes and potential pitfalls, further straining resources.
ACCeSS AI solution powered by Gen AI, primarily utilizes AWS Bedrock, S3 Storage, OpenSearch, DynamoDB, API Gateway, ECS and CloudFront to automate and accelerate clinical study setup.
Automated document generation
The solution extracts critical insights from protocols and regulatory documents with high accuracy, eliminating manual errors and accelerating document analysis. This ensures consistent generation of high-quality and compliant documentation, speeding up the setup process.
Accelerate Platform Setup
The solution enables faster development and testing iterations for repeatable study designs by automating generation of configuration code, metadata, mockups and validation and test scripts.
Standardization
The solution promotes standardization and minimizes effort duplication by automatically matching and retrieving reusable instruments from the eCOA library.
Highlights
- Automated document generation: The solution extracts critical insights from protocols and regulatory documents with high accuracy, eliminating manual errors and accelerating document analysis. This ensures consistent generation of high-quality and compliant documentation, speeding up the setup process.
- Accelerate Platform Setup: The solution enables faster development and testing iterations for repeatable study designs by automating generation of configuration code, metadata, mockups and validation and test scripts.
- Standardization: The solution promotes standardization and minimizes effort duplication by automatically matching and retrieving reusable instruments from the eCOA library. <As a point solution, how well does it integrate with existing flows><Will Brillio help with this> The Brillio team will assess the client ecosystem to perform the necessary integrations with the solution.
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This offering is ideal for Life sciences’ customers looking to accelerate their clinical study and eCOA platform setup.
Reach out to us at aws-marketplace@brillio.com OR Contact US to get started today!