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July 2026
CJEU, June 4, 2026: The Court provides clarification on the conformity assessment carried out by the distributor of medical devices
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Medical device law
Some devices that are CE marked according to one of the MD or AIMD directives can still be marketed after the date of application of the regulation.
Digital & E-health
The CNIL adopted by deliberation n° 2021-118 of 7 October 2021 (JORF 24 October 2021) a new reference framework aiming to "simplify the procedures".
Pharmaceutical law
The Council of State refers to the Constitutional Council the question of the conformity of the narcotics regulations on cannabis...
Since 2021, the amount of public R&D investment from which companies exploiting certain medicines have benefited is made available
Since 2021, a declaration of sales prices (net of discounts or taxes) must be made by operators or suppliers...
Regulation 2017/745 on medical devices (MDR) came into force on 26 May 2021 with the notable aim of evolving...
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