France and UK help Czech agency deliver on laws
This article was originally published in Clinica
Executive Summary
The UK and French regulatory agencies responsible for medical devices have joined forces in assisting the Czech regulator, SUKL, with the full implementation of the Medical Devices Directive, as well as with training on technical requirements. This is being carried out as part of the EU twinning programme where the more established EU member states assist the newer ones reach the same standards.
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