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Could Great Britain Recognise CE Devices Indefinitely?Regulatory

Could Great Britain Recognise CE Devices Indefinitely?

The MHRA is considering indefinite CE recognition in Great Britain. See what the proposal means for manufacturers, buyers and UKCA planning.

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22 Jul
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New EU Harmonised Standards for Medical Devices in 2026Regulatory

New EU Harmonised Standards for Medical Devices in 2026

See which EU medical device standards changed in 2026, when transitions apply, and what manufacturers and buyers should verify now.

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18 Jul
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EUDAMED Is Mandatory: What Medical Buyers Must CheckRegulatory

EUDAMED Is Mandatory: What Medical Buyers Must Check

EUDAMED is now mandatory for four EU modules. Here is what buyers should verify before shortlisting or purchasing medical devices.

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29 Jun
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EU MDR/IVDR 2026 Deadlines: What Manufacturers Must Do NowRegulatory

EU MDR/IVDR 2026 Deadlines: What Manufacturers Must Do Now

Key 2026 cutoff dates for EU MDR and IVDR legacy certificates are here. Manufacturers still transitioning must act now or lose EU market access.

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26 May
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