BY INDUSTRY
CROs
Every CRO is constantly seeking ways to enhance efficiency and deliver superior value to sponsors. Let IMC empower you with cutting-edge adherence technologies that automate tedious tasks and elevate your capabilities.
Solutions
Automate Tedious Work
Manual data collection and documentation can consume valuable time and resources, slowing trial progress and increasing the risk of errors. Med-ic® and eCap™ automate dose tracking and data collection effortlessly. Our devices seamlessly integrate with existing trial workflows, reducing manual intervention and allowing your team to focus on higher-value activities.
Make Data-Driven Decisions
Leverage IMC’s products and offer sponsors a compelling advantage that differentiates you from your competition. Our solutions enable real-time data insights, proactive intervention capabilities, and enhanced participant engagement—which all contributes to a smoother, more successful trial experience for sponsors and participants alike.
Drive Operational Efficiency
The CertiScan® Adherence Platform centralizes adherence data, empowering your team to analyze trends, monitor study progress, and generate on-demand reports with ease. Use real-time medication consumption rates to optimize resource allocation. Integration options allow our data and our features to work seamlessly within or alongside other clinical trial software systems and apps.
Learn More about the Products
that Power our Solutions
Consumer-quality software for clinical trials. Securely store, analyze, and action the data from smart packaging and other adherence devices. The CertiScan® Adherence Platform
includes web portals, mobile apps, developer tools, and a secure, central cloud.
ROI
Our experts have modelled the relationship between statistical power, sample size and medication adherence.
Their findings? For every 1% adherence increase, there can be a 2% reduction in trial size (N) while holding statistical power constant.
Considering that many trials currently only reach 50% adherence, there’s lots of room for improvement – and tremendous ROI.
Direct Savings from Reduced N
Processing a participant is expensive. Requiring a smaller sample size could amount to millions of dollars in savings.
Additional Weeks of Patent Protection
Smaller N means a faster trial, potentially by months. This could amount to tens of millions of dollars in additional revenue.
Compensate for Low or Slow Enrollments
It can be challenging to recruit enough participants - especially for niche diseases and even worldwide. Better data means fewer patients are needed overal.
Use Cases
Accurate data for transformative solutions.
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!)
This data feeds into the CertiScan® Adherence Platform and other software systems to power numerous solutions.
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.Detect and Treat:
- Medication non-adherence
- Medication misuse or abuse
- Temperature exposure and spoilage
- Expiry
- Tampering, fraud, and other lot or batch issues
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
- Conducting adaptive trials
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.Achieve efficiencies and reduce costs by:
- Automating data collection
- Basing site inventories on consumption rates
- Conducting adaptive trials
- Conducting decentralized trials
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
