Schreiner MediPharm extends its offering of smart packaging solutions by the new Smart Syringe Box. Thanks to integrated electronics, a wide variety of syringe packaging can now be digitized. The innovative solution enables automatic tracking of drug administration in clinical trials where precise therapy control is essential. Due to a special temperature monitoring feature, the Smart Syringe Box additionally provides benefits for temperature-sensitive biopharmaceuticals.

International clinical trials require maximum accuracy and efficient workflow but manual processes are often error-prone. Correct and regular administration of investigational drugs is essential but hard to monitor. Deviations from the dosing regimen can cause adulterated results and delays in time to market. A digital therapy monitoring solution such as the Smart Syringe Box provides crucial support in this case. Thanks to a cardboard layer with easy to open, perforated compartments, the removal of every single syringe can be precisely logged. The integrated electronics register relevant data such as removal time and the corresponding compartment in real time which are subsequently stored in the packaging and transmitted to a database via a smartphone app or Bluetooth.

A special benefit of the Smart Syringe Box is the option to integrate a temperature monitoring function. This is especially important for temperature-sensitive substances such as biopharmaceuticals as it enables tracking of the correct transportation and storage conditions. The adherence data generated not only support therapy tracking but also adjustments of individual therapy plans. The combination with specialized software enables central tracking, which facilitates the documentation and analysis
of the data.

Schreiner MediPharm adapts the integrated conductive lines precisely to the packaging design and the compartments to ensure reliable functionality and convenient handling. Scalable processes enable consistent automated production. The Smart Syringe Box offers numerous benefits for clinical trials: enhanced data quality, reduced failure rates due to non-adherence and optimized processes that reduce costs and shorten time to market of new drugs. At the same time, the need for manual documentation is eliminated, enabling higher flexibility and efficiency when conducting complex trials.