O T-DOC visualiza o custo de tudo, desde a esterilização e a mão de obra até os instrumentos e descartáveis, o que lhe fornece os dados de que você precisa para agir e executar um CSSD eficiente.

O T-DOC oferece alta segurança ao paciente e rastreabilidade precisa do instrumento, rastreando cada instrumento durante o ciclo de produção usando números de unidade exclusivos.

During sterile manufacturing, human operators pose the greatest risk for product contamination. To reduce microbiological and particulate contamination risks, aseptic techniques typically rely on either laminar flow equipment used within a cleanroom environment or barrier technology. Laminar flow equipment includes laminar flow hoods and biosafety cabinets (Class I, Class II, and Class III). Barrier technology includes restricted access barrier systems (RABS) and isolators.

Aragen’s goal was to see if their production process could be easily scaled up to larger, single-use bioreactors. Learn more about their findings.

Facing the dual challenge of boosting efficiency and reducing strain of staff, a leading sterilization provider in Japan has digitalized their sterile reprocessing.

Explore the future of pharmaceutical manufacturing with 4 key trends in sterile component transfer. From pre-validated solutions to manufacturing flexibility and increased automation, discover how industry leaders Getinge and West are shaping the landscape.

Discover how our DPTE® rapid transfer port, tested in collaboration with SafeBridge® Regulatory & Life Sciences Group, ensures personnel and environmental safety in pharmaceutical manufacturing facilities. Read the assessment of containment performance, validating the effectiveness of the DPTE® Alpha port against potentially hazardous active pharmaceutical ingredients.