With Covid accelerating time-to-market for medical devices, digital tools play a key role in managing converging priorities ...

Product design risks can be mitigated through digital commissioning strategies for device design that speed continuous design ...

Symphoni platform delivers real-time in-line quality assurance for medical devices, up to 320 parts per minute with 90% less ...

On February 2, 2026, the U.S. Food and Drug Administration (FDA) published its anticipated compliance program manual, ...

Given the highly infectious nature of the COVID pathogen, tests for the virus had to be quick, reliable and safe. The test ...

TekniPlex Healthcare, which utilizes advanced materials science expertise to help deliver better patient outcomes, will showcase its interventional and implantable device development, manufacturing, ...

Existing technology is being upcycled and deployed in new ways as companies seek to measure more data, more accurately.

Under earlier rules, drugmakers had to get a test licence from CDSCO to manufacture small quantities of drugs for research, examination or analysis.

Unified endpoint, platform engineering and hybrid cloud will help meet the military’s needs at the tactical edge.

Market valued at $76.50B in 2024, projected 9.75% CAGR growth driven by aerospace CMCs, EV batteries, semiconductor ...

Collaboration between development, quality, and purchasing departments is crucial for a secure supply chain, reducing risks and ensuring compliance. The Parenteral Drug Association's revised standard ...