By George Skampoulos, Associate LL.M A draft bill of the Ministry of Development that regulates, among other things, issues related to electronic fraud and the status of theft or accidental loss of credit and debit cards has already been put to consultation and is expected to come into force next month. The justification for the
titanium dioxide

Titanium Dioxide

By Aineias Spiliotis, January 2023 On 23 November 2022, press release No. 190/2022 was published on the website of the Court of Justice of the European Union announcing that the General Court annulled the Commission’s 2019 Delegated Regulation on the classification and labelling of titanium dioxide as a carcinogen when inhaled in the form of

ΑΙ, Metaverse & Ethical issues

By Evangelia Manika, Associate LL.B MSc. The use of AI in the metaverse, although it can bring many benefits, may also raise ethical issues as currently most AI is developed without ethical oversight. A key ethical implication surrounding AI in the metaverse is the bias of people creating AI algorithms so that those algorithms are
By Giorgos Skampoulos, Associate LL.M. By its decision No 37/2022, the Authority was called upon to rule on a complaint by a male father, who complained about the non-response of the complainant paediatrician to the right of access exercised by the latter in writing by means of an electronic message (sms), concerning medical data of
Digital Markets Act: Main Points

Digital Markets Act: Main Points

By Evangelia Manika New digital markets rules were agreed in record time (March 2022); in less than 2 years after the EU Commission’s Proposal in December 2020. Puts an end to unfair practices by companies that act as gatekeepers in the online platform economy -> Ensuring fair and open digital markets. The DMA covers ten
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

Food Safety Conference

EU Pharma Law Forum 2020

EU Pharma Law Forum


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