The importance of conscientious health data collection in European clinical trials

Published date17 January 2020
Subject MatterData Collection,Medical Devices,Life Sciences,EU,Big Data,Clinical Trials,Patient Privacy Rights,Medical Research,Information Management,R&D,Information Technology,Research and Development,Best Practices,Personal Data,Data Management,General Data Protection Regulation (GDPR),Pharmaceutical Industry,Data Processing Rules,Health Technology
AuthorPatrice Navarro
Law FirmHogan Lovells

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