What will the industry face or achieve in 2025? These trends will be critical in medical device cybersecurity.
An important facet of AI regulation is where in the supply chain AI should be regulated—specifically, whether to regulate the ...
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MHRA launches refreshed ILAP to speed up NHS drug accessThe pathway allows medicine developers to work with the regulators, the NHS and health technology assessment bodies.
The Centers for Medicare and Medicaid Services ("CMS") published a final notice outlining the processes and procedures for the Transitional ...
The U.S. Food and Drug Administration (FDA) recently issued two new guidance documents governing details of the Accelerated Approval ...
Centres of Excellence for Regulatory Science and Innovation (CERSIs) to help drive advancements in healthcare.Pioneering use of artificial intelligence (AI) could cut the time it takes to bring ...
MDR Certification Strengthens Resyca’s Leadership in Soft Mist Drug-Device Combination Products ENSCHEDE, NL / ACCESS ...
EQS-News: aap Implantate AG / Key word (s): Regulatory Approval/Miscellaneous Progress in the MDR process - aap receives MDR certificate 27.01.2025 / 14:00 CET/CEST The issuer is solely responsible ...
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