ARTICLES

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

Brianna Sporbert

Brianna Sporbert is the VP of Engineering and has been with Boyd Technologies since 2014. In her current role, she oversees commercialization of new products, the material sourcing and product development platforms, and enacting the company’s strategic growth plan. Brianna received a Bachelor of Science in Biomedical Engineering and a Master’s Degree in Business Administration from Western New England University. Previously, she worked as a research and development engineer with Flo Design Sonics where she assisted in the development of a novel acoustophoretic liquid filtration system that focused on blood filtration and biopharmaceutical processing. In her spare time, she enjoys coaching figure skating at the local rinks and mentoring young women in STEM.

Recent Articles

Recent Posts

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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White Paper: MedTech Supply Chain Strategies

Abstract

In today's evolving regulatory environment, supply chain transparency is a game-changing differentiator. Collaborating with manufacturing partners who have excellent supplier relationships and a deep understanding of materials can revolutionize the product development process. Even after a robust supply chain has been established, there are still hurdles in commercializing a medical device.

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Filtration Solution and Medical Membrane Device Development in IVD Applications: Current and Future Challenges

In Brief

The surging trends of an aging global population, the prevalence of chronic diseases, and the rise in outbreaks of infectious diseases have helped to expand the growth of the in vitro diagnostics (IVD) industry in the past several years. The demand for personalization and ease of use in IVD products for consumers and the influence of information technology have helped to cultivate more innovation in the industry.

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Demystifying Failure Mode and Effects Analyses (FMEAs) in Medical Device Manufacturing

In Brief

Failure Mode and Effects Analysis (FMEA) is a design review tool used to identify and correct all possible failures in a product, service, design or manufacturing process. This step-by-step approach was first initiated in the 1940s by the United States Army and further developed by NASA in the early 1960s.

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Challenges and Risks in Batch Bioprocessing

In Brief

Batch bioprocessing is the industry standard in biopharmaceutical production. Although the advancements in biomedical technology that have allowed for batch bioprocessing have been invaluable, some aspects of batch bioprocessing come with limits and challenges. 

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