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Both ethicists and lawyers accept that a provider – be it a researcher or a clinician – should provide sufficient information for a reasonable person to make an informed decision about whether they wish to go ahead with the proposed intervention or treatment.[1] They are bound to do so both because they have an ethical responsibility to preserve the ...
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To Consent or Not to Consent to Screening, That Is the Question
The objective of this article is to address the controversial question of whether consent is relevant for persons invited to participate in screening programs. To do so, it starts by presenting a case where the provided information historically has not been sufficient for obtaining valid informed consent for screening.
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Background The information provided to potential trial participants plays a crucial role in their decision-making. Printed participant information sheets for trials have received recurrent criticism as being too long and technical, unappealing and hard ...
Peter Knapp +11 more
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Exempting Health Research from the Consent Provisions of POPIA
The Protection of Personal Information Act 4 of 2013 (hereafter POPIA) has the potential to disrupt health research in South Africa. While the legal status quo is that broad consent by research participants is acceptable, POPIA requires specific consent ...
Donrich W Thaldar, Beverley A Townsend
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Context In vitro fertilisation (IVF) is now a common assisted reproductive technology (ART) procedure globally, with 8 million children alive today having been conceived utilising IVF.
Louis Taffs +2 more
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Validity conditions of civil legal act in new civil regulations of Republic of Moldova [PDF]
The most common legal facts that serve as a basis for the establishment of civil rights and obligations are civil legal acts.The civil legal act represents the most important source of civil rights and obligations, constituting a legal basis through ...
URSU, Viorica, CHIRIAC, Natalia
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Informed Consent and Consent Forms [PDF]
Informed consent is not often a significant part of a malpractice claim. To prevail on this issue, a jury or arbitrator must be convinced that the claimant would not have agreed to undergo the procedure if the possibility of occurrence of the complication that ultimately occurred, no matter how rare, had been disclosed.
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IntroductionConsent Labs is an Australian, youth-led, not-for-profit organization delivering comprehensive consent education. Workshops are co-designed by young people and delivered by near-to-peer facilitators in secondary and tertiary institutions. The
Melissa Kang +3 more
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Current innovations in the Czech pre-school education
In connection with the innovation in the Czech pre-school educa tion – placing two-year-old children in kindergarten, we identified the following: a) teachers’ attitude to accepting two-year-old children; b) the teachers’ reasons for rejecting two-year ...
Radmila Burkovičová
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STUDY AIMS: Little is known about the factors influencing patients’ response and decision rates to requests for general consent, designed to cover the use of health-related personal data and biological samples, in tertiary university hospitals. As such,
Cindy Allenbach +6 more
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