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Ophthalmological surgeries Handpieces: special points of attention
Are the EU Harmonised Standards valid also in the UK?
Compliance of COVID-19 protection equipment in the UK & NI: a brief explanation
All antigen and molecular COVID tests will need to pass validation
Artificial Intelligence and Software, you are very welcome to Great Britain
UKCA mark requirements postponed! Does it concern your products?
Services
UK Responsible Person (RP)
UK Consultancy, Legal & Training
UK Product Registration
––– Medical Devices & IVDs
––– Cosmetics
Technical Documentation
MEDICAL DEVICES
COSMETICS
––– Product Notification in the UK
––– UK Product Labelling
––– Product Formulation for the UK Market
––– Product Information File (PIF), Safety Assessor and CPSRs in the UK
––– Northern Ireland and the NI Protocol
IN-VITRO DIAGNOSTICS
UKCA
UK RP
UK RP for Cosmetics
UK RP for Medical Devices and In-Vitro Diagnostics
Blog
About us
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