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The IMDRF’s Standards Working Group issued final guidance on optimizing standards for regulatory use, noting that optimized standards offer a way to streamline regulatory processes as medical devices grow in complexity and international markets expand. Read More
Devicemakers marketing mobile health solutions or other software that help patients manage chronic conditions may see big benefits in coming years, new research suggests. Read More
The China Food and Drug Administration Wednesday announced registration fees for locally made and imported medical devices aimed at speeding up the processing of applications. Read More
The Indian government is waging a two-pronged attack on pricey implants, with the National Pharmaceutical Pricing Authority investigating reports of excessively high prices on orthopedic implants while a regional regulator office asks NPPA to look at cardiac stent pricing. Read More