ABOUT AARDEX GROUP

MEMS – it may sound like just another acronym, but in the world of clinical trials, it’s so much more. MEMS stands for Medication Event Monitoring System, a revolutionary technology transforming how medication adherence is monitored in clinical trials. With AARDEX Group’s MEMS technology, researchers now have access to an open ecosystem of medication adherence packaging and devices that seamlessly integrate with the industry-leading medication adherence software, MEMS AS. This powerful combination allows for real-time, objective data on medication-taking behavior, providing researchers with the insights they need to optimize treatment plans and dosages. But it’s not just about data – it’s about making a real impact on people’s lives. By leveraging the power of MEMS, researchers can gain a deeper understanding of medication adherence, helping to ensure that patients are getting the treatment they need to live their best lives. And with AARDEX Group’s unwavering commitment to innovation, the future of medication adherence monitoring looks brighter than ever.

The use of MEMS (Medication Event Monitoring System) technology for medication adherence monitoring is strongly supported by compelling evidence. MEMS technology involves electronic monitors embedded in medication packaging that record the date and time a participant opens the container to take medication.

Numerous studies have demonstrated the accuracy and effectiveness of MEMS in monitoring medication adherence. For instance, a systematic review of 25 studies found that MEMS was highly accurate in detecting medication adherence, with a median adherence rate of 81% across all studies.

Another study revealed that the use of MEMS technology significantly improved medication adherence rates in patients with HIV, leading to better treatment outcomes.

In addition, a meta-analysis of 17 randomized controlled trials indicated that the use of electronic monitoring devices such as MEMS resulted in a significant improvement in medication adherence compared to standard care.

Overall, the evidence unequivocally supports the use of MEMS technology in medication adherence monitoring. With its high accuracy and effectiveness, MEMS has the potential to enhance patient outcomes and yield new insights in medical research.

Here are some of the key benefits of utilizing a digital medication event monitoring system in clinical trials:

Improved accuracy: Compared to traditional methods such as self-reporting or pill counting, digital medication adherence solutions offer higher accuracy. These solutions can track medication adherence in real-time, providing precise and reliable data that can inform safety and efficacy calculations.

Increased efficiency: Digital medication adherence solutions can automate the monitoring process, saving time and resources for both participants and researchers. This can lead to more efficient clinical trials, ultimately accelerating the development of new treatments.

Better participant engagement: Digital medication adherence solutions can engage participants in their medication regimen by providing them with real-time feedback and coaching. This can help improve medication adherence rates, leading to better participant outcomes.

Enhanced data collection: Digital medication adherence solutions can collect a wealth of data on medication adherence patterns, offering valuable insights for future research. Researchers can identify trends and patterns in medication adherence, leading to better-informed decisions in the development of new treatments.

Increased flexibility: Digital medication adherence solutions can be utilized across a range of medication types and delivery methods, providing a scalable and flexible solution for clinical trials. This ensures that medication adherence is effectively measured and improved during clinical trials, ultimately leading to better outcomes for participants.

Poor medication adherence can significantly impact safety and efficacy calculations in clinical trials. Inaccurate safety and efficacy calculations can lead to inconclusive or misleading results, which can have severe consequences for patients.

When participants in a clinical trial do not adhere to their medication regimen as prescribed, it can affect the accuracy and reliability of the data collected. Non-adherence can lead to under-dosing or over-dosing, affecting the safety and efficacy of the medication being tested.

In terms of safety calculations, non-adherence can make it challenging to detect adverse events that may be related to the medication being tested. This can result in safety issues being overlooked or underestimated, which can harm patients.

In terms of efficacy calculations, non-adherence can make it challenging to accurately assess the effectiveness of the medication being tested. When participants do not take their medication as prescribed, the dosage levels may not be sufficient to achieve the desired therapeutic effect. This can lead to inaccurate efficacy calculations, undermining the validity of the trial results.