Ethical review, according to the ‘International Ethical Guidelines for Biomedical Research Involving Human Subjects ‘

Ethical review, according to the ‘International Ethical Guidelines for Biomedical  Research Involving Human  Subjects ‘ (CIOMS, 2002): Ethical review. The ethical review committee is responsible for safeguarding the rights, safety, and well-being of the research subjects. Scientific review and ethical review cannot be separated: scientifically unsound research involving humans as

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European Medicines Agency: Posting of clinical trial summary results in European Clinical Trials Database (EudraCT) to become mandatory for sponsors as of 21 July 2014

European Medicines Agency – – Posting of clinical trial summary results in European Clinical Trials Database (EudraCT) to become mandatory for sponsors as of 21 July 2014: European Medicines Agency – – Posting of clinical trial summary results in European Clinical Trials Database (EudraCT) to become mandatory for sponsors as

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Onverwachte bevindingen

Check out our new educational tool. IRB Primer: Incidental and Secondary Findings http://t.co/ptqQIe9ieF More to come. — Bioethics Commission (@bioethicsgov) April 16, 2014 Just posted: Primers for Practitioners on Incidental & Secondary Findings. First up – the Clinician Primer: http://t.co/PTj4fQUV3a — Bioethics Commission (@bioethicsgov) May 5, 2014 The Direct-to-Consumer Provider

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Overzicht van ‘Ethische Commissies Psychologie’ in Nederland

[Updated: 4 november 2014] Mede omdat niet al het onderzoek met mensen aan de Wet medisch wetenschappelijk onderzoek met mensen getoetst hoeft te worden, hebben de Nederlandse universiteiten zogenaamde Ethische Commissies Psychologie ingesteld om psychologisch en gedragswetenschappelijk onderzoek op ethische aspecten te beoordelen. Op één na zijn al deze commissies op

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