Informed Consent

Informed consent is a process for getting permission before conducting a healthcare intervention on a person, for conducting some form of research on a person, or for disclosing a person's information. A health care provider may ask a patient to consent to receive therapy before providing it, a clinical researcher may ask a research participant before enrolling that person into a clinical trial, and a researcher may ask a research participant before starting some form of controlled experiment. Informed consent is collected according to guidelines from the fields of medical ethics and research ethics. An informed consent can be said …

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Publications

UNEP: United Nations Environment Programme · 26 November 2024 English

Documents Background Participants This is a capacity-building workshop for national focal points of the MEAs and the Montevideo Programme V to facilitate the implementation of Biodiversity and Chemicals/ Waste Multilateral …

the 1998 Rotterdam Convention on the Prior Informed Consent Procedure for certain Hazardous Chemicals Disposal Rotterdam Convention on the Prior Informed Consent Procedure for Certain Hazardous Chemicals


WHO: World Health Organization · 20 November 2024 English

iv, 20 p.

acutely ill infants and children; obtaining informed consent from parents; and the efficient development


GAIA: Global Alliance for Incinerator Alternatives · 20 November 2024 English

This would be important in order to complete the drafting and agreement on treaty text including all the core obligations needed to end plastic pollution across the life cycle of …

developed and implemented an interim Prior Informed Consent procedure; - proposed 14 additional chemicals


WHO: World Health Organization · 17 November 2024 English

vii, 11 p.

communities throughout the data life cycle. • Informed consent is a critical component for the ethical use and communicated clearly in advance. • Informed consent should be as specific and granular as possible appropriate informed consent model (e.g. specific, broad, tiered or dynamic informed consent) depends depends upon the individual/local context. • Informed consent should be supported by governance frameworks specific purpose for human genome data use, informed consent to broad categories of human genome data


WHO: World Health Organization · 17 November 2024 English

[‎vii]‎, 44 p.

guidance across 138 countries (so far) globally. Informed consent, regulatory authorization and ethical oversight


WHO: World Health Organization · 15 November 2024 English

vi, 113 p.

provided by all participants. Individual informed consent should be sought from participants, such


Institut Veblen · 14 November 2024 English

These measures will ensure the the adoption of a regulation on the mitiga- reciprocity of standards in the European mar- tion of the imported environmental and ket, encouraging a shift …

opportunities will arise. The revision of the Prior Informed Consent (PIC) regulation6 presents another chance 8 https://echa.europa.eu/regulations/prior-informed-consent/legislation https://agriculture.ec.europa


The South Centre · 13 November 2024

The Supreme Court found that in the absence in the Bill of mitigatory measures -as allowed by the TRIPS Agreement- and of a working definition of the term “microorganism”, there …

peoples and local communities’ rights to prior informed consent, to benefit sharing, and to guaranteeing their


World Bank Group · 13 November 2024 English

This study uses a cluster randomized controlled trial to evaluate the impact of a nationwide malaria prevention advertising campaign delivered through social media in India. Ads were randomly assigned at …

providing study details to obtain individuals’ informed consent for their participation in the research. Only


World Bank Group · 12 November 2024 English

necessary a process to obtain free, prior and informed consent. ESS6 - Biodiversity Conservation and Sustainable


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