Luer connectors are commonly used in the medical field, but their uniform design across multiple device types has resulted in serious misconnection issues.
White Papers and Case Studies
Partner with an ISO 22301-certified supplier like Qosina to ensure supply chain resiliency, technical quality and cost efficiency.
Supply chain breakdowns in product quality, delivery or availability are major disruptions in the medical device supply industry.
This white paper has been updated to reflect the most recent developments in European Union Medical Device Regulation (MDR) and In Vitro Device Regulation (IVDR) and to bring the current situation into focus.
The European Union Medical Device Regulation (MDR) and In Vitro Device Regulation (IVDR) is a set of standards that governs the production and distribution of medical devices in Europe.
Our newly released white paper discusses the criticality of updating your medical device risk analysis throughout the product lifecycle, conducting proper complaint investigation and designing for human factors.
The high stress of an emergency room or ICU creates an environment where the probability of human error spikes dramatically, adding a layer of risk to an already-tense situation.
