Oct 19, 2022 EU Pharma & Medical Device Regulation 2023 By Marco de Morpurgo Nicola Landolfi Our EU Life Sciences Regulatory team led by Marco de Morpurgo and Nicola Landolfi have produced a guide on EU Pharma & Medical Device...
May 17, 2021 Interactions with healthcare professionals – launch of the new DLA Piper interactive compliance site for pharmaceutical companies By Marco de Morpurgo Andrzej Balicki, Ph.D. Ethical relations with healthcare professionals are of vital importance for pharmaceutical companies. Cooperation with them results in a...
Apr 23, 2020 Clinical trials during the COVID-19 pandemic: A global guide By Dr Kokularajah Paheenthararajah After weeks of intensive collaboration and inspiring contributions from more than 100 Life Sciences enthusiasts across five continents,...
Mar 20, 2023 Extended transition period gives medical device industry extra time to comply with EU MDR By Marco de Morpurgo Nicola Landolfi A much-awaited extension of the MDR transition period became effective today with the publication of Regulation (EU) 2023/607 in the...
Nov 23, 2020 Telehealth around the world: A global guide By Greg Bodulovic Stephanie Wang Marco de Morpurgo Eliza Saunders +1 more... Show less The COVID-19 pandemic has caused healthcare systems around the globe to rapidly, and in some cases, radically rethink the delivery of...
Jan 25, 2022 Update: DLA Piper Global COVID-19 Vaccine Guide for Employers By Marco de Morpurgo DLA Piper’s Life Sciences team has updated our recent vaccine guide for employers. The changes include significant updates to several...
Oct 05, 2021 Update: DLA Piper Global COVID-19 Vaccine Guide for Employers By Marco de Morpurgo DLA Piper’s Life Sciences team has updated our recent vaccine guide for employers. The changes include the additions of Sweden and...
May 25, 2021 Launch of DLA Piper Global COVID-19 Vaccine Guide for Employers By Pilar Menor Marco de Morpurgo As the scientific response to the COVID-19 pandemic develops, many employers are considering what their approach should be to the issues...
Mar 16, 2021 Wearable technologies: legal lifecycle of taking a new product to market By Eliza Saunders Marco de Morpurgo 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...
Feb 06, 2023 Clinical trials in the EU: mandatory CTIS procedures and new transparency requirements from 31 January 2023 By Marco de Morpurgo Nicola Landolfi On 31 January 2023, the new Clinical Trials Information System (CTIS) established by Regulation (EU) 536/2014 on clinical trials (CTR)...
Nov 15, 2022 Clinical Trials and Privacy Matters: A Cross-border Guide By Marco de Morpurgo This week our Life Sciences team published the first edition of its Cross-border Guide to Clinical Trials and Privacy. The Guide will...
Apr 03, 2020 European Commission proposes one-year postponement of MDR application date By Mark Franklin Marco de Morpurgo Paula Gonzalez de Castejón Llano-Ponte Nicola Landolfi +1 more... Show less Following an informal heads-up on 25 March 2020, today the European Commission adopted a proposed regulation to postpone by one year the...
Oct 06, 2022 New IFPMA/EFPIA guidance on social media and digital channels By Marco de Morpurgo Carlotta Busani The International Federation of Pharmaceutical Manufacturers and Associations (IFPMA) and the European Federation of Pharmaceutical...
Sep 20, 2022 Italian adapts national medical device framework to MDR and IVDR By Marco de Morpurgo Carlotta Busani Italy enacted legislation to adapt the national framework governing medical devices and in vitro-diagnostic medical devices to the MDR...
Jul 14, 2022 European Commission proposes new rules on blood, tissues, and cells By Marco de Morpurgo Nicola Landolfi Today, the European Commission adopted a proposal for a new Regulation on standards of quality and safety for substances of human origin...
Jan 31, 2022 New EU Clinical Trial Regulation to take effect from today By Marco de Morpurgo Carlotta Busani Today, the new EU Clinical Trials Regulation (Regulation (EU) No 534/2014 – “CTR”) becomes applicable. The CTR introduces a unified...