EUCROF, the European CRO Federation, is the initiator of the first transnational "Code of Conduct", aimed at ensuring the compliance of clinical research service organisations (CROs) with the European General Data Protection Regulation (GDPR). For the success of this initiative, it is important to have the contribution of all stakeholders involved in clinical research programmes, i.e. clinical trial sponsors (pharmaceutical and biotech industry, medical device manufacturers, academics and hospital), patient associations, and health professionals. Hence, EUCROF, with the very active support of its members (national CRO associations) and associate members, has formally launched an important consultation programme for these stakeholders.
For further details, please read the article published by TIC Pharma in France.
