Experiences With Secondary Use of Qualitative Data—First Results of a Survey Carried out in the Context of a Feasibility Study Concerning Archiving and Secondary Use of Interview D... by Diane Opitz, Reiner Mauer

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Biobanks: Archives or Resources? Their Secondary Use for Forensic Purposes—A Systematic Review by Giulia Sguazzi, Giulia Fasani, Filippo Renò, Sarah Gino

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Reviewing Mass-Observation: The Archive and its Researchers Thirty Years on by Dorothy Sheridan

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Legal problems with the transformation of waste into the products (a case study of phosphogypsum) by M. A. Buchakova, N. D. Vershilo, O. A. Dizer

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Ensuring Purpose Limitation in Large-Scale Infrastructures with Provenance-Enabled Access Control by Shizra Sultan, Christian D. Jensen

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Born again by Dragana Antonović, Vidan Dimić

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The Time Efficiency Gain in Sharing and Reuse of Research Data by Tessa E. Pronk

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Public Interest, Health Research and Data Protection Law: Establishing a Legitimate Trade-Off between Individual Control and Research Access to Health Data by Mark J Taylor, Tess Whitton

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Responsible data sharing in international health research: a systematic review of principles and norms by Shona Kalkman, Menno Mostert, Christoph Gerlinger, Johannes J. M. van Delden, Ghislaine J. M. W. van Thiel

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The Secondary Use of Data to Support Medication Safety in the Hospital Setting: A Systematic Review and Narrative Synthesis by Navila Talib Chaudhry, Bryony Dean Franklin, Salmaan Mohammed, Jonathan Benn

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Health screening and its association with emergency department visits and related costs among home-dwelling older adults by Jonna-Carita Kanninen, Hannu Kautiainen, Anu Holm

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Challenges arising when seeking broad consent for health research data sharing: a qualitative study of perspectives in Thailand by Phaik Yeong Cheah, Nattapat Jatupornpimol, Borimas Hanboonkunupakarn, Napat Khirikoekkong, Podjanee Jittamala, Sasithon Pukrittayakamee, Nicholas P. J. Day, Michael Parker, Susan Bull

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Parental perspectives on retention and secondary use of neonatal dried bloodspots: a Dutch mixed methods study by Marleen E. Jansen, Lion J. M. van den Bosch, Marjolein J. Hendriks, Mariska M. J. Scheffer, Marie-Louise Heijnen, Conor M. W. Douglas, Carla G. van El

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Health data between improving health(care) and fuelling the data economy by Tjasa Petrocnik

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Regulating the Secondary Use of Data for Research: Arguments Against Genetic Exceptionalism by Andrea Martani, Lester Darryl Geneviève, Christiane Pauli-Magnus, Stuart McLennan, Stuart McLennan, Bernice Simone Elger, Bernice Simone Elger

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Ethics practices associated with reusing health data: an assessment of patient registries by Olmo R. van den Akker, Susanne Stark, Daniel Strech

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Sharing genomic data from clinical testing with researchers: public survey of expectations of clinical genomic data management in Queensland, Australia by Miranda E. Vidgen, Sid Kaladharan, Eva Malacova, Cameron Hurst, Nicola Waddell

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Australian general practitioner perceptions to sharing clinical data for secondary use: a mixed method approach by Richard J. Varhol, Sean Randall, James H. Boyd, Suzanne Robinson

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Multi-label text classification via secondary use of large clinical real-world data sets by Sai Pavan Kumar Veeranki, Akhila Abdulnazar, Diether Kramer, Markus Kreuzthaler, David Benjamin Lumenta

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Open access and its potential impact on public health – A South African perspective by Adéle Strydom, Juanita Mellet, Jeanne Van Rensburg, Ignatius Viljoen, Anastasios Athanasiadis, Michael S. Pepper

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