Artykuły

In pharmaceutical production, maintaining equipment uptime is essential for operational efficiency and process safety. Particularly in cleanroom environments, unplanned downtime can disrupt workflows, increase overhead costs, and in some cases contribute to delays in drug availability.

In the ever-evolving landscape of medical technology, ensuring the safety and performance of surgical equipment is paramount. The IEC 60601-2-41:2021 (Edition 3) standard sets forth the particular requirements for the basic safety and essential performance of surgical luminaires and luminaires for diagnosis.

Modern operating rooms are high-stakes environments where every minute counts. An unexpected issue with critical equipment like the operating table can disrupt schedules and even jeopardize patient safety.

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.

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

Branża farmaceutyczna nieustannie poszukuje innowacji, które poprawiają bezpieczeństwo, wydajność i precyzję produkcji leków. Jedną z takich rewolucyjnych technologii, która znacząco wpłynęła na branżę, jest system DPTE®, wprowadzony w latach 60. ubiegłego wieku W tym artykule przedstawiamy historię i ewolucję technologii DPTE®, podkreślając jej kluczową rolę w produkcji farmaceutycznej oraz bogate doświadczenie, jakie firma Getinge wnosi na rynek po 60 latach pracy w tej dziedzinie.

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.

A new pre-validated wash rack, enabling the staff at Fujirebio to create a standardized cleaning process of multi-use bioreactors which saves time in their important work to produce more antibodies used in cancer diagnostics.

Ensure guidance of your unexperienced staff and adapt to different user competency levels while maintaining a high and consistent quality level of the sterile production.

When a 68-year old Finnish man’s heart stopped beating, the close proximity to the only regional, non-university hospital in the Nordic region with Extracorporeal Membrane Oxygenation (ECMO) service helped to save him.

Bacterial infections acquired in the operating room are the most common form of healthcare-associated infection. Using digital door signs to minimize in-and-out traffic during surgeries effectively reduces this infection risk.