I3CGlobal FDA INSPECTION BANGALORE, INDIA, March 14, 2025 /EINPresswire / -- Indian pharmaceutical, nutraceutical, and medical devic ...

Standards such as ISO 13485 (Medical Device QMS), FDA 21 CFR Part 820 (Medical Device Manufacturing), and IEC 60601 (Medical Electrical Equipment Safety) dictate design controls, validation testing, ...

R&D Engineer : Medical Device & Regulations - Full time - 100% REMOTE Must Have Technical/Functional Skills Good Knowledge of Medical Devices & QMS (ISO 13485, 21 CFR Part 820) and familiarity ...

Agenda 21 is a comprehensive plan of action to be taken globally, nationally and locally by organizations of the United Nations System, Governments, and Major Groups in every area in which human ...

The World Anti-Doping Code (Code) is the core document that harmonizes anti-doping policies, rules and regulations within sport organizations and among public authorities around the world. It works in ...

This advertisement has not loaded yet, but your article continues below. The Prince Edward Island Regulatory and Appeals Commission (IRAC) announced a one-cent change to regular gas prices overnight, ...

The Defense Department said Friday that it's cutting about 5,400 probationary workers starting next week and will put a hiring freeze in place. It comes after staffers from the Department of ...