EUMDR & EUIVDR The webinar and Q&A session
Following the successful EU wide webinar on MDR and IVDR organized in Amsterdam by the Alliance of Life Sciences Law Firms, in which our partner Ioanna Michalopoulou presented the relevant Greek framework and current legislative status, we share with you the link through which you can access the recording of the seminar’s proceedings.
PRRC: newly introduced requirement of MDR/IVDR
November 2022By Evangelia Manika, Associate PRRC stands for person responsible for regulatory compliance.In particular, PRRC is a qualified regulatory expert that is responsible, among others, for ensuring that the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released. According

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EU Pharma Law Forum 2020

EU Pharma Law Forum

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Health Stakeholders Ecosystem

EC Regulation of Crypto-assets


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