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Learn how the use of color coding in medical device design can help ensure the safe and effective delivery of treatments and medications...

Mechanical hose barb connections, which consist of the hose barb, tubing and retention device, are ubiquitous in single-use systems (SuS). They look deceptively simple, but the process of bringing all three elements...

Picture a life that starts in Kiev, Ukraine, takes a detour through the Air Force, and arrives at the forefront of healthcare innovation in the USA. This is my story, and it's nothing short of extraordinary...

Single-use assemblies are designed with many connection points, or engagements. This refers to the places where two components are assembled, such as tubing on a hose barb, or two sanitary flanges connected with a gasket and clamp...

Discover how USP <800> affects original equipment manufacturers (OEMs) in designing medical devices for hospitals. Ensure compliance and safety with facility requirements...

Sanitary fittings are known in the industry under several names. These include, but may not be limited to, sanitary flange, sanitary coupler, ferrule, tri-clamp, tri-clover, hygienic union, or sometimes just TC for short...

In vitro diagnostic (IVD) instrumentation is used in a variety of healthcare applications to detect many different human elements related to patient diagnosis and treatment. IVD instruments are used for sample preparation, blood chemistry, therapeutic dru

There are many factors to consider when selecting an appropriate bag chamber for a single-use system to support your bioprocess. The task can seem overwhelming, so it is important to lean on stringent procedures to ensure a successful outcome...

When choosing a quick disconnect connector for a medical device, there are several important factors that should considered. Learn how compatibility, sterilization, durability and safety play a critical role in ensuring device functionality...

The development of a medical device is a complex and extensive process. Rigorous design planning and controls will mitigate risks that lead to failed verification testing or other delays in the project...

The proposed restriction of per- and polyfluoroalkyl substances (PFAS) is a growing topic of conversation in the bioprocess and biopharma industry. Regulatory bodies have concerns regarding the hazardous properties of these chemicals as they are increasin