about
Quality and safety of genetic testing in Australia and New Zealand: a review of the current regulatory framework.Clinical ethics support services in New Zealand-tailoring services to meet the needs of doctors.Towards a practical definition of professional behaviour.3-Fluoro-benzoic acid-4-acetyl-pyridine (1/1) at 100 K.Gender agenda: let's track women's trial participation.Health data research in New Zealand: updating the ethical governance framework.The experiences of pregnant women in an interventional clinical trial: Research In Pregnancy Ethics (RIPE) study.Pregnancy and the Culture of Extreme Risk Aversion.Consent and the ethical duty to participate in health data research.Benefits to research subjects in international trials: do they reduce exploitation or increase undue inducement?Daily decision-making about food during pregnancy: a New Zealand study.Prenatal diagnosis and abortion for congenital abnormalities: is it ethical to provide one without the other?Response to open peer commentaries on "Prenatal diagnosis and abortion for congenital abnormalities: is it ethical to provide one without the other?".IAB Presidential address: "Searching for Justice".Is sex-selective abortion morally justified and should it be prohibited?'Fair benefits' accounts of exploitation require a normative principle of fairness: response to Gbadegesin and Wendler, and Emanuel et al.HIV international clinical research: exploitation and risk.In Favor of a No-Consent/Opt-Out Model of Research With Clinical SamplesPregnancy, Vulnerability, and the Risk of Exploitation in Clinical ResearchJustice in Health Research: What is the Role of Evidence-Based Medicine?Gender Inequities in Health Research: An Australian PerspectiveGender and trust in medicine: Vulnerabilities, abuses, and remediesPopulações especiais: vulnerabilidade e proteçãoWhen is sex-specific research appropriate?Data and tissue research without patient consent: A qualitative study of the views of research ethics committees in New ZealandWhere is the human in the data? A guide to ethical data useAdjusting the focus: A public health ethics approach to data researchFrom protectionism to inclusion: A New Zealand perspective on health-related research involving adults incapable of giving informed consent
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P50
description
researcher ORCID ID = 0000-0003-2666-9557
@en
name
Angela Ballantyne
@ast
Angela Ballantyne
@en
Angela Ballantyne
@es
Angela Ballantyne
@nl
type
label
Angela Ballantyne
@ast
Angela Ballantyne
@en
Angela Ballantyne
@es
Angela Ballantyne
@nl
prefLabel
Angela Ballantyne
@ast
Angela Ballantyne
@en
Angela Ballantyne
@es
Angela Ballantyne
@nl
P21
P31
P496
0000-0003-2666-9557