In the EU, the AI Act has been approved, carrying significant implications for medical device, technology, and pharmaceutical firms. In the US, ...
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OCT Medical Devices 2025: biggest regulatory requirement issues ‘start at the site level’When conducting a clinical investigation, meeting regulatory requirements is predicated on factors such as the quality of ...
The Food and Drug Administration (FDA) of the Philippines has warned the public against purchasing two beauty soaps by ...
MDR Certification Strengthens Resyca’s Leadership in Soft Mist Drug-Device Combination Products ENSCHEDE, NL / ACCESS ...
Dr. Sara Brenner, who has been FDA CDRH's in vitro diagnostics chief medical officer, is serving as acting commissioner of the agency.
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