Monitoring and documentation of temperature, humidity and shock in pharmaceutical logistics
Most pharmaceuticals must be continuously transported and stored at defined upper and lower temperature and humidity limit values, along the entire supply chain. A violation of these predefined upper and lower limit values can lead to irreversible alterations of the active ingredients or the composition of the medicaments.
However, not only medicaments and their active ingredients are endangered. Minus temperatures or extreme temperature fluctuations can also cause damage to containers or medical instruments. The consequence is the threat of spoilage of the entire goods, financial losses and damage to reputation.
In GxP-compliant quality management, the control of the entire cold chain, from production to delivery, is therefore a prerequisite, in order not only to ensure product quality, but also to prevent financial losses and damage to your reputation in the pharmaceutical industry.
With the testo 184 data loggers, your products can be protected from unnoticed gaps in the cold chain, and the entire distribution path monitored and documented simply, securely and compliantly with all common standards, guidelines and regulations.