New regulations challenged how surgical kits were tracked and processed across 15 U.S. sites. Discover how one team balanced ...

Discover how digitized workflows and real-time verification are helping streamline clinical trial packaging, reduce complexity, and improve quality in a high-stakes, time-sensitive environment.

Rapid prototyping has taken the medical device industry by storm, but there are pros and cons that device developers need to ...

Whether youre refining existing protocols or developing new ones, this guide serves as a valuable resource for ensuring safe, ...

Medical device manufacturers must maintain a detailed Device History Record (DHR) to meet FDA requirements and ensure ...

PolyPeel™ peelable polyester heat shrink tubing streamlines catheter manufacturing with speed, precision, and sustainability, offering a PFAS-free alternative to FEP for safer, more efficient medical ...

Autoinjectors revolutionized drug delivery, but innovation is shifting toward oral, wearable, and alternative platforms.

In the pharma/biotech and medical device industries, the audit trail is important to have for accountability, data integrity, repeatability to create an event for investigation, and regulatory ...

Ophthalmic medical devices address significant global health needs, as over 2.2 billion people face vision impairment, much of which is preventable or treatable. These devices range from low-risk ...

Legacy medical devices often remain in use long after their operating systems, firmware, and security protections have become outdated, creating significant challenges for manufacturers. These devices ...

The development of prefilled syringes (PFS) and auto-injectors (AI) is essential for precise and reliable medication delivery. Ensuring safety, efficacy, and usability involves a combination of ...