The EUs Medical Devices Regulation (MDR) has introduced a new level of rigor. A sophisticated, yet practical, strategy is ...

One major change introduced by the EU MDR compared to the former European directives is the inclusion of products without an ...

Optical micro overmolding combines micro molding with lead-frame or insert processes to achieve precision, clarity, and ...

Learn how to be more proactive by implementing robust PFAS testing and control strategies to safeguard patient health, ...

Sharp is advancing clinical trial packaging by digitizing its operations with Tulip’s no-code platform. In an industry where trials can span a decade and cost millions, Sharp’s focus is on reducing ...

The European Union's revised Annex 1 guidelines for sterile medicinal products, effective August 2023, mandate a significant shift in how manufacturers approach risk management and contamination ...

The European Union's Good Manufacturing Practice (EU GMP) Annex 1 has fundamentally redefined the standards for manufacturing sterile medicinal products globally. While the goal—enhancing public ...

The digital revolution that resulted in the Internet of Things (IoT), Internet of Medical Things (IoMT), Software as a Medical Device (SaMD), and connected devices permeating the healthcare ...

The project will create at least 200 new, full-time jobs over the next three years and retain 1,704 existing full-time positions. The Commonwealth is supporting the project with $1.5 million in state ...

AI-assisted symptom recognition and pattern matching leverages machine learning to analyze vast amounts of medical data, including patient histories, clinical notes, and research publications, to ...