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Transparenz in der klinischen Forschung: Welchen Beitrag leistet die neue EU-Verordnung 536/2014?

Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz, 2023, Vol.66 (1), p.52-59

Strech, Daniel

2023

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Improving the trustworthiness, usefulness, and ethics of biomedical research through an innovative and comprehensive institutional initiative

PLoS biology, 2020-02, Vol.18 (2), p.e3000576-e3000576

2020

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Institutional dashboards on clinical trial transparency for University Medical Centers: A case study

PLoS medicine, 2023-03, Vol.20 (3), p.e1004175-e1004175

2023

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Transparency in clinical research: What contribution does the new EU Regulation 536/2014 make?

Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz, 2023-01, Vol.66 (1), p.52-59

Strech, Daniel

2023

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Reporting of retrospective registration in clinical trial publications: a cross-sectional study of German trials

BMJ open, 2023-04, Vol.13 (4), p.e069553-e069553

2023

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Preclinical efficacy studies in investigator brochures: Do they enable risk-benefit assessment?

PLoS biology, 2018-04, Vol.16 (4), p.e2004879-e2004879

2018

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Stakeholders’ views on an institutional dashboard with metrics for responsible research

PloS one, 2022-06, Vol.17 (6), p.e0269492-e0269492

2022

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Ethical issues in public health surveillance: a systematic qualitative review

BMC public health, 2017-04, Vol.17 (1), p.295-295, Article 295

2017

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The representation of patient experience and satisfaction in physician rating sites. A criteria-based analysis of English- and German-language sites

BMC health services research, 2010-12, Vol.10 (1), p.332-332, Article 332

2010

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Frequency of multiple changes to prespecified primary outcomes of clinical trials completed between 2009 and 2017 in German university medical centers: A meta-research study

PLoS medicine, 2023-10, Vol.20 (10), p.e1004306-e1004306

2023

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Publication rates in animal research. Extent and characteristics of published and non-published animal studies followed up at two German university medical centres

PloS one, 2019-11, Vol.14 (11), p.e0223758-e0223758

2019

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Implementation of data access and use procedures in clinical data warehouses. A systematic review of literature and publicly available policies

BMC medical informatics and decision making, 2020-07, Vol.20 (1), p.157-157, Article 157

2020

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Empirical studies on how ethical recommendations are translated into practice: a cross-section study on scope and study objectives

BMC medical ethics, 2023-01, Vol.24 (1), p.2-2, Article 2

2023

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Animal Study Registries: Results from a Stakeholder Analysis on Potential Strengths, Weaknesses, Facilitators, and Barriers

PLoS biology, 2016-11, Vol.14 (11), p.e2000391-e2000391

2016

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An integrated conceptual framework for evaluating and improving 'understanding' in informed consent

Trials, 2017-10, Vol.18 (1), p.482-482, Article 482

2017

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Why are so few patients rating their physicians on German physician rating websites? A qualitative study

BMC health services research, 2018-08, Vol.18 (1), p.670-670, Article 670

2018

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Current practice of public involvement activities in biomedical research and innovation: a systematic qualitative review

PloS one, 2014-12, Vol.9 (12), p.e113274-e113274

2014

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The Public's Awareness of and Attitude Toward Research Biobanks - A Regional German Survey

Frontiers in genetics, 2018-05, Vol.9, p.190-190

2018

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The Full Spectrum of Clinical Ethical Issues in Kidney Failure. Findings of a Systematic Qualitative Review

PloS one, 2016-03, Vol.11 (3), p.e0149357-e0149357

2016

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Web-based survey among animal researchers on publication practices and incentives for increasing publication rates

PloS one, 2021-05, Vol.16 (5), p.e0250362-e0250362

2021

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Routinely collected data for randomized trials: promises, barriers, and implications

Trials, 2018-01, Vol.19 (1), p.29-29, Article 29

2018

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The bench is closer to the bedside than we think: Uncovering the ethical ties between preclinical researchers in translational neuroscience and patients in clinical trials

PLoS biology, 2018-06, Vol.16 (6), p.e2006343-e2006343

2018

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Data protection-compliant broad consent for secondary use of health care data and human biosamples for (bio)medical research: Towards a new German national standard

Journal of biomedical informatics, 2022-07, Vol.131, p.104096-104096, Article 104096

2022

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Measurement challenges and causes of incomplete results reporting of biomedical animal studies: Results from an interview study

PloS one, 2022-08, Vol.17 (8), p.e0271976-e0271976

2022

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Results availability and timeliness of registered COVID-19 clinical trials: interim cross-sectional results from the DIRECCT study

BMJ open, 2021-11, Vol.11 (11), p.e053096-e053096

2021

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Transparenz in der klinischen Forschung: Welchen Beitrag leistet die neue EU-Verordnung 536/2014?

Improving the trustworthiness, usefulness, and ethics of biomedical research through an innovative and comprehensive institutional initiative

Institutional dashboards on clinical trial transparency for University Medical Centers: A case study

Transparency in clinical research: What contribution does the new EU Regulation 536/2014 make?

Reporting of retrospective registration in clinical trial publications: a cross-sectional study of German trials

Preclinical efficacy studies in investigator brochures: Do they enable risk-benefit assessment?

Stakeholders’ views on an institutional dashboard with metrics for responsible research

Ethical issues in public health surveillance: a systematic qualitative review

The representation of patient experience and satisfaction in physician rating sites. A criteria-based analysis of English- and German-language sites

Frequency of multiple changes to prespecified primary outcomes of clinical trials completed between 2009 and 2017 in German university medical centers: A meta-research study

Publication rates in animal research. Extent and characteristics of published and non-published animal studies followed up at two German university medical centres

Implementation of data access and use procedures in clinical data warehouses. A systematic review of literature and publicly available policies

Empirical studies on how ethical recommendations are translated into practice: a cross-section study on scope and study objectives

Animal Study Registries: Results from a Stakeholder Analysis on Potential Strengths, Weaknesses, Facilitators, and Barriers

An integrated conceptual framework for evaluating and improving 'understanding' in informed consent

Why are so few patients rating their physicians on German physician rating websites? A qualitative study

Current practice of public involvement activities in biomedical research and innovation: a systematic qualitative review

The Public's Awareness of and Attitude Toward Research Biobanks - A Regional German Survey

The Full Spectrum of Clinical Ethical Issues in Kidney Failure. Findings of a Systematic Qualitative Review

Web-based survey among animal researchers on publication practices and incentives for increasing publication rates

Routinely collected data for randomized trials: promises, barriers, and implications

The bench is closer to the bedside than we think: Uncovering the ethical ties between preclinical researchers in translational neuroscience and patients in clinical trials

Data protection-compliant broad consent for secondary use of health care data and human biosamples for (bio)medical research: Towards a new German national standard

Measurement challenges and causes of incomplete results reporting of biomedical animal studies: Results from an interview study

Results availability and timeliness of registered COVID-19 clinical trials: interim cross-sectional results from the DIRECCT study

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