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 integration, demanding early collaboration to ensure manufacturability, ...

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

The revised EU GMP Annex 1 prioritizes a CCS. Learn how to holistically manage microbial, particulate, chemical, and ...

Implementing the EU GMP Annex 1 requires a holistic, evolutionary Contamination Control Strategy built on standardization, ...

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 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 ...

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 ...