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Home » Topics » Regulatory

Regulatory
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Australia amends first tranche of broad medical device regulations

Jan. 17, 2020
By Tamra Sami
PERTH, Australia – Australia’s Parliament has passed the first tranche of medical device regulations reforms that follow a number of consultations over the last two years.
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Regulatory front for Jan. 17, 2020

Jan. 17, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies.
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FDA approves Ozempic to reduce MACE in adults with type 2 diabetes and heart disease

Jan. 17, 2020
1-16-Mojo-lens-hero.png

Mojo Vision’s smart contact lens wins breakthrough device designation from FDA

Jan. 16, 2020
By Meg Bryant
The U.S. FDA has granted breakthrough device designation to Mojo Vision Inc. for its first-of-a-kind true smart contact lens. The Mojo Lens, which features “invisible computing” and a built-in display, enables people to get timely information without having to look away from what they are doing or glance at a screen.
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Regulatory front for Jan. 16, 2020

Jan. 16, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies.
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Cardiovascular.png

Cardiologists pushing back on rule to judge appropriateness of stenting

Jan. 16, 2020
By Mark McCarty
Device makers only can watch when cardiologists grapple with federal agency officials over device utilization. However, cardiologists are punching back hard against a rule used to judge whether a coronary artery stent is appropriately used, thus ensuring these devices won’t suffer a significant drop in utilization.
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China promotes real-world evidence in R&D and approval with new guidelines

Jan. 16, 2020
By Elise Mak
BEIJING – China has released guidelines to promote the use of real-world evidence (RWE) in drug development and reviews.
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Regulatory front for Jan. 16, 2020

Jan. 16, 2020
The latest global regulatory news, changes and updates affecting biopharma.
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European Commission grants marketing authorization for Isturisa

Jan. 16, 2020
Map of Europe

EU posts guidelines for medical device cybersecurity

Jan. 15, 2020
By Nuala Moran
LONDON – The European Commission has published new guidelines on cybersecurity for medical devices, putting flesh on the bones of the requirements in the Medical Device Regulation (MDR) that comes into force in May.
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