Maximizing Clinical Data Quality with eCOA & Rater Training
We recognise gathering the highest quality data is paramount to the success of clinical trials, which means partnering with a trusted provider is crucial. Designed specifically to enhance the sensitivity of outcome measures, our eCOA services increase the reliability of Clinical Outcome Assessment data, giving your trial the best chance of success.
Our comprehensive offering
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Simplify Your Process: Enjoy a comprehensive end-to-end solution that includes eCOA, scale management, rater training, and central monitoring, eliminating the need to rely on multiple providers for your clinical trials.
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Reduce Costs Automatically: Discover how our proprietary tests and innovative anti-risk tools such as AQUA can efficiently flag errors, helping you save on costs and streamline your clinical operations.
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Achieve Exceptional Speed and Quality: Experience unparalleled clinical operational quality and speed with our commitment to delivering First Patient First Visit (FPFV) without delay. We can take you from contract signing to trial initiation in as little as 8 weeks, with accelerated options available to meet your needs.
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How it Works
Read below to understand our full offering
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What We Offer
Read below to understand a clear walk-through of our products and services
eCOA: Digital bespoke questionnaires and universally recognised clinical scales
Capture the high-quality neurocognitive data you need for your study quickly and efficiently using a single platform. Available in multiple languages and across multiple devices, our eCOA solution enables you to collect valid data across all your sites with patients from different countries, as well as self-administration to support decentralised trial without rater presence. All responses are collected electronically, scored in near real-time, then uploaded to a secure database, giving you immediate access to your data.Read more about our eCOA offering here.
Rater Training: Simplifying the Burdensome
Cambridge Cognition understands that conventional rater training can often be cumbersome and inefficient. To address this, we have developed an advanced rater qualification and management program that ensures raters are well-prepared to conduct cognitive assessments to the highest standards, all while simplifying the training process.
Our method is founded on a comprehensive insight into the typical challenges and error patterns faced by raters. We customize our training to align with the experience levels of each rater, which reduces the training burden and accelerates the timeline for study start-up. With Cambridge Cognition, you can trust that your raters will be thoroughly equipped to deliver exceptional results efficiently.
Scale Management: Speed, reliability, and reputation
The right assessment scales not only facilitate the evaluation of therapeutic effectiveness but also enhance the reliability of trial results. Poorly chosen or poorly managed scales can lead to delayed timelines, increased costs, and compromised data quality, ultimately affecting the overall integrity of the trial. Our dedicated clinical operation team fosters collaborative relationships with license holders, translation specialists, and other essential partners to ensure that you receive accurate and timely delivery of the scales you need. These positive relationships are evidenced by our consistently excellent client Net Promoter Scores.
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Central Monitoring: Save up to 60% compared to other providers
In the complex landscape of clinical research, even small rater errors can lead to significant discrepancies, impacting the reliability of the results. Effective central monitoring not only helps to catch these errors early but also reinforces the credibility of the clinical findings.
At Cambridge Cognition we implement systematic checks and balances, so researchers can enhance the accuracy and value of their data. Using our unique and proprietary tools, we combine the efficiency of automated quality assurance with the precision of human oversight to provide high quality review data at up to 60%* of the cost of traditional providers.
Contact Our Experts
Contact us about any part of our overall eCOA offering and our team will be happy to help
Frequently Asked Questions
Learn More About Our Services
How does your platform support rater training?
- Standardized Training Modules: Tailored to meet study-specific requirements.
- On-Demand Access: Training materials available online for convenient access.
- Continuous Support: Resources for retraining and support throughout the study.
Why should we choose your eCOA platform?
- Flexibility: Supports multiple assessment types, including cognitive, CNS-specific, and quality-of-life evaluations.
- Real-time Data Access: Immediate access to insights and data for faster decision-making.
- Regulatory Compliance: Built to comply with FDA, EMA, and other global regulatory standards.
- Seamless Integration: Compatible with existing trial systems and workflows, ensuring minimal disruption.
Is your solution customisable to our study needs?
Yes! Our platform can be fully customized to align with your study’s protocols, assessment types, and workflow requirements. From user interfaces to reporting formats, we ensure the solution fits seamlessly into your clinical trial.
What scales are supported across all your services?
We pride ourselves on being CNS experts (and beyond!) and this includes supporting a large range of scales. Reach out to our team and explain your needs, and we will work on an implementation plan just for you to make sure you get the best outcome on your clinical trial.
What kind of technical support is available?
- A dedicated account manager for your project.
- A responsive helpdesk for troubleshooting.
- Training and resources for study teams and participants.
How long does implementation take?
Implementation timelines depend on the complexity of your study. However, our experienced team ensures a streamlined setup process, with most studies up and running within 4–8 weeks.
Can your platform accommodate global, multi-site trials?
Absolutely. Our solution is designed for scalability and supports multilingual capabilities, region-specific requirements, and centralized data management to streamline global trials.
Do you offer any trial or demonstration of the platform?
Yes! We can provide a tailored demonstration or a pilot setup to showcase how our platform meets your specific needs. Contact us to schedule your demo today.