CONTENTS We will briefly see what is difference between ethics and legislation, what kind of ethical guidelines and regulations are linked to HESs. We will also discuss about the role of ethics committee and informed consent in the framework of a HES. LEARNING OBJECTIVES Ethical guidelines for health surveys GDPR requirements for health surveys What is informed consent and why it is needed The recording of the session is available here
Most professional and institutional, national, and international guidelines and ethical codes for re...
There are several ethical guidelines and international legal regulations on the requirements that sh...
Informed consent is both a legal and ethical doctrine. As an ethical doctrine, informed consent is b...
This document describes the procedures and criteria that will be used to identify/recruit research p...
Health policy and systems research (HPSR) is increasingly funded and undertaken as part of health sy...
The documents address: Detailed information on the informed consent procedures that are implement...
Medical researchers are ethically and legally required to inform participants and get written permis...
For several decades Clinical trials are a "back-bone" of new drug development. Even if Ethical codic...
Informed consent can be considered, without any doubt, as a central issue in current bioethics and i...
© The Author 2017. Health policy and systems research (HPSR) is increasingly funded and undertaken a...
Ethics committees now require that individuals give informed consent to much health services researc...
CONTENTS Fundamentals of Health information ethics Fundamentals of GDPR Build-in Ethics and GDP...
Ethics committees now require that individuals give informed consent to much health services researc...
peer reviewede-Health data is sensitive and consenting to the collection, processing, and sharing in...
The predominant view is that a study using health data is observational research and should require ...
Most professional and institutional, national, and international guidelines and ethical codes for re...
There are several ethical guidelines and international legal regulations on the requirements that sh...
Informed consent is both a legal and ethical doctrine. As an ethical doctrine, informed consent is b...
This document describes the procedures and criteria that will be used to identify/recruit research p...
Health policy and systems research (HPSR) is increasingly funded and undertaken as part of health sy...
The documents address: Detailed information on the informed consent procedures that are implement...
Medical researchers are ethically and legally required to inform participants and get written permis...
For several decades Clinical trials are a "back-bone" of new drug development. Even if Ethical codic...
Informed consent can be considered, without any doubt, as a central issue in current bioethics and i...
© The Author 2017. Health policy and systems research (HPSR) is increasingly funded and undertaken a...
Ethics committees now require that individuals give informed consent to much health services researc...
CONTENTS Fundamentals of Health information ethics Fundamentals of GDPR Build-in Ethics and GDP...
Ethics committees now require that individuals give informed consent to much health services researc...
peer reviewede-Health data is sensitive and consenting to the collection, processing, and sharing in...
The predominant view is that a study using health data is observational research and should require ...
Most professional and institutional, national, and international guidelines and ethical codes for re...
There are several ethical guidelines and international legal regulations on the requirements that sh...
Informed consent is both a legal and ethical doctrine. As an ethical doctrine, informed consent is b...
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