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Join date: Oct 9, 2020
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Feb 26, 2023 ∙ 2 min
Getting Users to answer Post Market Surveillance Questionnaires: Tips for Manufacturers (AI created)
Post market surveillance is a critical aspect of the medical device industry. It involves monitoring the safety and effectiveness of...
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Jan 30, 2023 ∙ 1 min
What's up with the certification of Class IIb/III devices under the MDR?
End of May 2025, devices certified under the MDD can no longer be sold or distributed in EU - less than 28 months to go. Tick-tock,...
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May 26, 2021 ∙ 3 min
Medical Device Manufacturers: Align your Ducks and make MDR a Friend for Innovation
It's May 26, 2021 and seems that the sun is still shining somewhere behind the clouds despite much anxiousness regarding the new MDR...
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