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.

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

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, ...

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 ...

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 ...

Early recognition and mitigation of drug and device integration difficulties are critical to the success of combination products. The collaborative effort in development cannot be overstated.

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

Discover how a top medical device manufacturer accelerated product launch by digitizing assembly processes, streamlining ...

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

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 ...