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Our EU Life Sciences Regulatory team led by Marco de Morpurgo and Nicola Landolfi have produced a guide on EU Pharma & Medical Device...
Cortex - Life Sciences Insights
24 results for:
"Marco de Morpurgo"
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Ethical relations with healthcare professionals are of vital importance for pharmaceutical companies. Cooperation with them results in a...
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After weeks of intensive collaboration and inspiring contributions from more than 100 Life Sciences enthusiasts across five continents,...
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A much-awaited extension of the MDR transition period became effective today with the publication of Regulation (EU) 2023/607 in the...
The COVID-19 pandemic has caused healthcare systems around the globe to rapidly, and in some cases, radically rethink the delivery of...
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DLA Piper’s Life Sciences team has updated our recent vaccine guide for employers. The changes include significant updates to several...
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DLA Piper’s Life Sciences team has updated our recent vaccine guide for employers. The changes include the additions of Sweden and...
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As the scientific response to the COVID-19 pandemic develops, many employers are considering what their approach should be to the issues...
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Wearable devices is a term used for electronic devices that can be worn on the body, either as an accessory like a watch or a pair of...
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On 31 January 2023, the new Clinical Trials Information System (CTIS) established by Regulation (EU) 536/2014 on clinical trials (CTR)...
This week our Life Sciences team published the first edition of its Cross-border Guide to Clinical Trials and Privacy. The Guide will...
Following an informal heads-up on 25 March 2020, today the European Commission adopted a proposed regulation to postpone by one year the...
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The International Federation of Pharmaceutical Manufacturers and Associations (IFPMA) and the European Federation of Pharmaceutical...
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Italy enacted legislation to adapt the national framework governing medical devices and in vitro-diagnostic medical devices to the MDR...
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Today, the European Commission adopted a proposal for a new Regulation on standards of quality and safety for substances of human origin...
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Today, the new EU Clinical Trials Regulation (Regulation (EU) No 534/2014 – “CTR”) becomes applicable. The CTR introduces a unified...