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	<title>The Embassy of Good Science - User contributions [en]</title>
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	<updated>2026-04-15T05:28:48Z</updated>
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		<id>https://embassy.science:443/wiki-wiki/index.php?title=Resource:1690d5b9-7ddb-4f9b-95ec-1222a0b4f8cb&amp;diff=6262</id>
		<title>Resource:1690d5b9-7ddb-4f9b-95ec-1222a0b4f8cb</title>
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		<updated>2021-03-31T10:22:03Z</updated>

		<summary type="html">&lt;p&gt;0000-0002-8319-3658: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{Resource&lt;br /&gt;
|Resource Type=Guidelines&lt;br /&gt;
|Title=Guidelines for Tailoring the Informed Consent Process in Clinical Studies&lt;br /&gt;
|Is About=These guidelines are designed to assist in the development or revision of the consent process for use in clinical trials involving human participants. These guidelines do not address issues related to informed consent in clinical practice.&lt;br /&gt;
The guidelines have been developed by the i-CONSENT consortium. i-CONSENT (H2020, Grant Agreement number 741856) is an EU-funded H2020 project that aims to improve the information that individuals receive when deciding whether or not to participate in clinical trials.&lt;br /&gt;
|Important For=Clinical researchers; All stakeholders in research; Clinical ethics consultants; Ethics committee members; medical researchers; Research subjects; sponsors; Pharma Industry; Regulators&lt;br /&gt;
}}&lt;br /&gt;
{{Link&lt;br /&gt;
|Has Link=https://i-consentproject.eu/wp-content/uploads/2021/03/Guidelines-for-tailoring-the-informed-consent-process-in-clinical-studies-2.pdf&lt;br /&gt;
}}&lt;br /&gt;
{{Related To}}&lt;br /&gt;
{{Tags&lt;br /&gt;
|Related To Research Area=LS 07.11 - Medical ethics&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>0000-0002-8319-3658</name></author>
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	<entry>
		<id>https://embassy.science:443/wiki-wiki/index.php?title=Resource:1690d5b9-7ddb-4f9b-95ec-1222a0b4f8cb&amp;diff=6178</id>
		<title>Resource:1690d5b9-7ddb-4f9b-95ec-1222a0b4f8cb</title>
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		<updated>2021-03-25T13:56:27Z</updated>

		<summary type="html">&lt;p&gt;0000-0002-8319-3658: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{Resource&lt;br /&gt;
|Resource Type=Guidelines&lt;br /&gt;
|Title=Guidelines for Tailoring the Informed Consent Process in Clinical Studies&lt;br /&gt;
|Is About=These guidelines are designed to assist in the development or revision of the consent process for use in clinical trials involving human participants. These guidelines do not address issues related to informed consent in clinical practice.&lt;br /&gt;
The guidelines have been developed by the i-CONSENT consortium. i-CONSENT (H2020, Grant Agreement number 741856) is an EU-funded H2020 project that aims to improve the information that individuals receive when deciding whether or not to participate in clinical trials.&lt;br /&gt;
|Important For=Clinical researchers; All stakeholders in research; Clinical ethics consultants; Ethics committee members; medical researchers; Research subjects; sponsors; Pharma Industry; Regulators&lt;br /&gt;
}}&lt;br /&gt;
{{Link&lt;br /&gt;
|Has Link=http://doi.org/10.5281/zenodo.4563938&lt;br /&gt;
}}&lt;br /&gt;
{{Related To}}&lt;br /&gt;
{{Tags&lt;br /&gt;
|Related To Research Area=LS 07.11 - Medical ethics&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>0000-0002-8319-3658</name></author>
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		<id>https://embassy.science:443/wiki-wiki/index.php?title=Resource:1690d5b9-7ddb-4f9b-95ec-1222a0b4f8cb&amp;diff=6175</id>
		<title>Resource:1690d5b9-7ddb-4f9b-95ec-1222a0b4f8cb</title>
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		<updated>2021-03-25T13:52:27Z</updated>

		<summary type="html">&lt;p&gt;0000-0002-8319-3658: Created page with &amp;quot;{{Resource |Resource Type=Guidelines |Title=Guidelines for Tailoring the Informed Consent Process in Clinical Studies |Is About=These guidelines are designed to assist in the...&amp;quot;&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{Resource&lt;br /&gt;
|Resource Type=Guidelines&lt;br /&gt;
|Title=Guidelines for Tailoring the Informed Consent Process in Clinical Studies&lt;br /&gt;
|Is About=These guidelines are designed to assist in the development or revision of the consent process for use in clinical trials involving human participants. These guidelines do not address issues related to informed consent in clinical practice.&lt;br /&gt;
The guidelines have been developed by the i-CONSENT consortium. i-CONSENT (H2020, Grant Agreement number 741856) is an EU-funded H2020 project that aims to improve the information that individuals receive when deciding whether or not to participate in clinical trials.&lt;br /&gt;
|Important For=Clinical researchers; All stakeholders in research; Clinical ethics consultants; Ethics committee members; medical researchers; Research subjects; sponsors; Pharma Industry; Regulators&lt;br /&gt;
}}&lt;br /&gt;
{{Link&lt;br /&gt;
|Has Link=http://doi.org/10.5281/zenodo.4563938&lt;br /&gt;
}}&lt;br /&gt;
{{Related To}}&lt;br /&gt;
{{Tags}}&lt;/div&gt;</summary>
		<author><name>0000-0002-8319-3658</name></author>
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	<entry>
		<id>https://embassy.science:443/wiki-wiki/index.php?title=User:0000-0002-8319-3658&amp;diff=6172</id>
		<title>User:0000-0002-8319-3658</title>
		<link rel="alternate" type="text/html" href="https://embassy.science:443/wiki-wiki/index.php?title=User:0000-0002-8319-3658&amp;diff=6172"/>
		<updated>2021-03-25T13:40:05Z</updated>

		<summary type="html">&lt;p&gt;0000-0002-8319-3658: create user page&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{S_User | Jaime |  Fons-Martínez }}&lt;/div&gt;</summary>
		<author><name>0000-0002-8319-3658</name></author>
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