Knowledge Center

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.

There is strong evidence supporting the use of MEMS (Medication Event Monitoring System) technology in medication adherence monitoring. MEMS technology involves the use of electronic monitors embedded in medication packaging that record the date and time a patient opens the container to take medication.

Numerous studies have demonstrated the accuracy and effectiveness of MEMS in medication adherence monitoring. For example, 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 found that the use of MEMS technology significantly improved medication adherence rates in patients with HIV, leading to better treatment outcomes.

Furthermore, a meta-analysis of 17 randomized controlled trials found that the use of electronic monitoring devices like MEMS was associated with a significant improvement in medication adherence compared to standard care.

Overall, the evidence strongly supports the use of MEMS technology in medication adherence monitoring. With its high accuracy and effectiveness, MEMS can help improve patient outcomes and drive new insights in medical research.

Using a digital medication adherence solution in clinical trials has several benefits. Here are some of the key reasons:

Improved accuracy: Digital medication adherence solutions are more accurate than traditional methods such as self-reporting or pill counting. 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 process of monitoring medication adherence, saving time and resources for both participants and researchers. This can lead to more efficient clinical trials and ultimately accelerate the development of new treatments.

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

Enhanced data collection: Digital medication adherence solutions can collect a wealth of data on medication adherence patterns, providing valuable insights that can inform future research. This can help researchers 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 used across a range of medication types and delivery methods, providing a flexible and scalable solution for clinical trials. This can help ensure that medication adherence is

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.