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MJ Medica Consulting Ltd
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MJ Medica Consulting Ltd
About
Services
Regulatory Insights
Resources
Contact MJ Medica
About
Services
Regulatory Insights
Resources
Contact MJ Medica
UK Market Access Michael Murphy 23/10/2026 UK Market Access Michael Murphy 23/10/2026

CE Marking in Great Britain: MHRA Confirms Indefinite Recognition

The UK Government has confirmed indefinite recognition of EU MDR and IVDR CE-marked medical devices in Great Britain. Here is what changes - and what manufacturers still need to do.

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Technical Documentation Michael Murphy 23/10/2026 Technical Documentation Michael Murphy 23/10/2026

The GSPR Checklist Should Be an Evidence Map Not a Tick Box Exercise

A GSPR checklist should do more than confirm compliance. Used properly, it becomes a traceable evidence map linking each applicable requirement to the method of conformity and the objective evidence that supports it.

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MJ Medica Consulting Ltd

Regulatory Affairs & Quality Consulting

Medical Devices | IVD | SaMD & AI | Pharmaceuticals

EU MDR | EU IVDR | UK MDR | FDA | ISO 13485 | ISO 14971

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