CoolBlue® AI Temperature Sensing Technology eliminates the need for separate expensive loggers. It may be directly integrated into our smart packages, allowing for dose-level monitoring and reporting of temperature history, temperature excursions and product status.
Features
Tracks exposures from -15 C to 65 C (5 F to 149 F)
Logs the entire temperature history of each package
Tracks total amounts of time exposed to particular temperatures
Automatically computes pharma-relevant MKT values
OK/NOK status lights support safe medication use
3+ years of operational life span
Sensor components are non-primary contact surfaces
Compatible with GMP and GCP workflows
Product Details
CoolBlue® AI Temperature Sensing Technology equipped smart packages (Med-ic®) track temperature continuously throughout the cold chain, in addition to recording date and time of product removal from the smart package.
Patients can easily see if the product is safe to use with OK/NOK status displays on the package, reducing any concerns about temperature or product integrity. Additional data displays and actions are available to patients through the CertiScan® companion app, helping them keep track of their adherence progress.
CoolBlue® AI is an ideal add-on for clinical trials that involve injectable or temperature sensitive that involve smart blister packaged medication (such as the Med-ic Syringe® Pack). It is also valuable for commercial products where adherence and temperature control are crucial.
Smart packaging is the ideal data source: it is accurate, automatic, and passive. There is no extra effort on the participant’s part since they were going to take a dose anyways (or not - which smart packaging can also detect!)
Inappropriate medication use is widespread in clinical research. This can harm individual participant outcomes, jeopardize trial outcomes, and cause hidden errors that are only discovered post market or after publishing (such as a poorly titrated dosage or undiscovered side effect).
Our solutions make it easy to detect and treat these harmful issues. Many protective features are automatic, such as mobile reminders, misuse alerts, targeted coaching.
Shorter trials that reach their endpoints more quickly can gain weeks or months of additional patent protection. This can amount to substantial additional revenue.
Our solutions help studies reach last dose, last participant sooner.
Improve timelines by:
Automating data collection
Replacing diaries and ePRO with smart packaging
Letting CertiScan preprocess and analyze data
Integrating CertiScan with RTSMs, EDCs, and other platforms
Clinical trials are becoming increasingly complex and expensive. Certain activities in a protocol seem straightforward on paper, but in practice can translate into dozens of hours of site work.
Use our solutions to help eliminate needless overhead and streamline processes.
New, technology-first strategies are transforming clinical trials. DCTs, participant diversity initiatives, and AI tools are changing from “nice-to-haves” into “must-haves”.
Our solutions are modern tools for modern trials that can help researchers and other stakeholders gain and maintain an advantage.
Adopt CertiScan and smart packaging to:
Meet FDA trial modernization guidelines
Model PK and PD with adherence data
Satisfy internal and external innovation requirements
Build accurate, objective datasets for use in AI models, participant diversity initiatives, DCT tools, and more
Publish unique studies that stand out in the literature
Software
Explore The CertiScan® Platform
Our industry leading CertiScan® Adherence Platform unlocks the value of your adherence data. CertiScan® handles data retrieval, storage, analysis, and reporting.
CertiScan® is a full suite that includes web portals, desktop software, mobile apps, developer tools, and a unifying cloud backend. You can use the entire platform as a whole, or a just subset that satisfies your particular needs.
Our mission is to create adherence-focused technologies that enable safer, faster, more efficient, and more innovative clinical research.There’s an IMC solution that will transform your next trial. Don’t wait, start the conversation with our team now.We’ll reach out in order to: