white paper & case studies

White Papers and Case Studies

The Case for Just-In-Time Inventory Management
Partner with an ISO 22301-certified supplier like Qosina to ensure supply chain resiliency, technical quality and cost efficiency.
How to Improve Resiliency in the Medical Device Supply Chain

Supply chain breakdowns in product quality, delivery or availability are major disruptions in the medical device supply industry.

The Clock Is Ticking: Will Notified Body Capacity for the EU MDR Affect You?
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.
What Can the Medical Device Industry Learn from the Boeing 737 MAX 8 Crashes?
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.
Overcoming Barriers of Adopting ISO 80369

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.

Actionable Steps to Eliminate Small-Bore Connector Misconnection | Adopting ISO 80369

Luer connectors are commonly used in the medical field, but their uniform design across multiple device types has resulted in serious misconnection issues.