Do you have a cybersecurity postmarket surveillance plan ready for your next 510(k)/De Novo/PMA submission?
June 29, 2023
FDA guidance calls for postmarket surveillance plans and cybersecurity assessments.
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June 29, 2023
FDA guidance calls for postmarket surveillance plans and cybersecurity assessments.
June 26, 2023
Protect your clinical trials from cybersecurity threats.
June 22, 2023
The EU’s Medical Device Regulations mean changing the way you develop implantable medical devices.
June 14, 2023
For Breakthrough Devices, FDA’s new TAP Pilot program could change the game.
June 13, 2023
Take immediate action to avoid the most common deficiencies.