Reinforcing core ASTM-based packaging validation methods for medical devices and their operational relevance.

A first-of-its-kind collaboration between Boston Medical Center and Takeda finds that most regulated medical waste is ...

Medline turned to Ranpak Holdings Corp. to eliminate a growing bottleneck at pack-out. The company now picks directly into a ...

Insights from the SPMC on how success depends on recognizing the different roles plastics play, validating alternatives ...

The company's investment in a "Mechanistic Integrity" manufacturing model aims to reduce variability and improve scalability ...

GENIE is a real-time, LLM-agnostic intelligence engine that converts complex regulations into machine-executable logic for ...

For clean medicine brand Genexa, its recent packaging redesign reflects a shift toward helping parents quickly find what they ...

Healthcare packaging is evolving to balance patient safety, regulatory demands, and environmental responsibility. Discover ...

Packaging producers must prepare now as compliance deadlines for Extended Producer Responsibility (EPR) programs near seven states. To stay ahead of the changing obligations and avoid potential ...

Whether a material is compatible with different sterilization methods is a serious concern for medical device manufacturers. Whether a material is compatible with different sterilization methods is a ...

In June of 2016, the FDA issued a final rule, Use of Symbols in Labeling, which allows for the use of symbols in all medical device labeling without additional explanatory text. The move was made in ...

This content was written and submitted by the supplier. It has only been modified to comply with this publication’s space and style. ELMACH, a provider of solid-dose packaging technologies, highlights ...