ARTICLES

Technical articles focused on the design, development, and commercialization of single-use regulated devices. 

Recent Articles

Applications of Flexible Materials in Health Care

In Brief

Flexible materials combined with emerging technologies are at the forefront of health care innovations. Guiding recent advances are cost concerns, mass-production, and improved patient outcomes.

 

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7 Steps to Effectively Dual Source a Supply Chain for Medical Devices

In Brief

Dual sourcing is considered a hassle by some traditional medical device manufacturers. After all, the procurement process is faster and more straightforward when you only have to issue purchase orders and receive components from one vendor. Adding a second supplier to your list of approved vendors takes time and creates additional work for your accounts payable staff. 

 

In reality, dual sourcing can be accomplished efficiently and can be a win-win solution if you follow a few key measures. Below is a look at some of the benefits of dual sourcing and your seven-step guide to effectively dual sourcing a supply chain for medical devices. 

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Development of Paper-Based Microfluidics Devices for Point-of-Care Testing

In Brief

Developments in the in vitro diagnostics (IVD) industry have been driven by global trends such as the prevalence of chronic diseases, an aging population, the increase in the occurrence of contagious diseases, and the influence of technology innovators. These trends, plus the desire for ease of use and a general acceptance of personalized care by consumers in developed and developing countries, have influenced IVD developments.

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Application of Molecularly Imprinted Polymers in POC Diagnostics

In Brief

Standard disposable point-of-care diagnostic (POCD) devices are making a positive impact on patient-based healthcare settings worldwide. These devices are convenient and economical, and they provide rapid results. Both clinicians and patients use them to diagnose a range of conditions.

But in certain situations, these diagnostic devices have limitations.

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6 Filtration Challenges in Downstream Biopharmaceutical Production

In Brief

Membranes and membrane processes are efficient filtration tools in the manufacturing of biopharmaceutical products. These tools continue to evolve in response to new therapies and processing methods. The membranes used in separation and purification are beginning to play an even more important role as market demand for monoclonal antibodies (mAbs) and other gene and cell culture therapies have expanded in recent years. The global mAb therapeutics market is projected to grow from almost US$ 95.6 billion in 2017 to US$ 174.2 billion by 2026.

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