Responsibility: Recommendations - Revision history

Isabelle: /* Responsibilities */

2021-03-24T12:57:25Z

‎Responsibilities

Isabelle: /* Responsibilities */

2021-03-10T12:02:28Z

‎Responsibilities

Isabelle at 11:32, 10 March 2021

2021-03-10T11:32:24Z

Isabelle at 08:32, 21 January 2021

2021-01-21T08:32:24Z

Isabelle: /* Rules, guidelines */

2021-01-19T14:18:20Z

‎Rules, guidelines

Isabelle: /* Rules, guidelines */

2021-01-19T14:17:48Z

‎Rules, guidelines

Isabelle: /* Responsibilities */

2021-01-13T11:48:46Z

‎Responsibilities

Isabelle: /* Responsibilities */

2021-01-13T09:01:56Z

‎Responsibilities

Isabelle: /* Responsibilities */

2021-01-13T08:58:25Z

‎Responsibilities

Isabelle: /* Responsibilities */

2021-01-13T08:57:13Z

‎Responsibilities

← Older revision		Revision as of 12:57, 24 March 2021
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	Make sure that the designated responsible party is qualified to do so. One respondent of our [https://elifesciences.org/articles/62212 survey] pointed out: “Neither the researchers, inclusively the PI's are in a place to take responsibility for work with technologies that they do not understand.”		Make sure that the designated responsible party is qualified to do so. One respondent of our [https://elifesciences.org/articles/62212 survey] pointed out: “Neither the researchers, inclusively the PI's are in a place to take responsibility for work with technologies that they do not understand.”
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		+	[[Start_here\|Go back to menu]]

← Older revision		Revision as of 12:02, 10 March 2021
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	Define responsibilities precisely. Who will be responsible (the CF, the user, the PI or another scientist) regarding the experimental design, sample preparation, data acquisition, data storage, data analysis, documentation and publication? The ones who carry the responsibility for doing or supervising/checking each step must be clearly defined before starting any experiments (as well as shared responsibilities). This will prevent that suboptimal results/procedures could be proceeding unidentified. Discuss these items during a meeting with the user and fill out a [[:File:Responsibility distribution.docx\|'''responsibility table''']].		Define responsibilities precisely. Who will be responsible (the CF, the user, the PI or another scientist) regarding the experimental design, sample preparation, data acquisition, data storage, data analysis, documentation and publication? The ones who carry the responsibility for doing or supervising/checking each step must be clearly defined before starting any experiments (as well as shared responsibilities). This will prevent that suboptimal results/procedures could be proceeding unidentified. Discuss these items during a meeting with the user and fill out a [[:File:Responsibility distribution.docx\|'''responsibility table''']].

−	Make sure that the designated responsible party is qualified to do so. One respondent of our survey pointed out: “Neither the researchers, inclusively the PI's are in a place to take responsibility for work with technologies that they do not understand.”	+	Make sure that the designated responsible party is qualified to do so. One respondent of our [https://elifesciences.org/articles/62212 survey] pointed out: “Neither the researchers, inclusively the PI's are in a place to take responsibility for work with technologies that they do not understand.”

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-Give the users documents that they should read and sign.
+Discussing how to responsibilities and duties will be shared between CF and user allows transparency and helps keeping optimal research quality standards. The result of this discussion should also be put in writing, read and signed.
 == Rules, guidelines ==
-State the rules of the facility, give guidelines. Explain about CF procedures, communication, safety, pricing. Give information about [[Data management: Recommendations|'''data management''']] (data naming convention, data saving, data transfer, data long-term storage)
+Provide written guidelines defining the rules of the facility. Explain about CF procedures, communication, safety, pricing. Give information about [[Data management: Recommendations|'''data management''']] (data naming convention, data saving, data transfer, data long-term storage). Also explain the duties of the users.
 == Responsibilities ==
-Define responsibilities precisely. Who will be responsible (the CF, the user, the PI or another scientist) regarding the experimental design, sample preparation, data acquisition, data storage, data analysis, documentation and publication? The ones who carry the responsibility for doing or supervising/checking each step must be clearly defined before starting any experiments (as well as shared responsibilities). This will prevent that suboptimal results/procedure are not identified and go on as if they were fine. Discuss it all together at a meeting and fill up a [[:File:Responsibility distribution.docx|'''responsibility table''']].
+Define responsibilities precisely. Who will be responsible (the CF, the user, the PI or another scientist) regarding the experimental design, sample preparation, data acquisition, data storage, data analysis, documentation and publication? The ones who carry the responsibility for doing or supervising/checking each step must be clearly defined before starting any experiments (as well as shared responsibilities). This will prevent that suboptimal results/procedures could be proceeding unidentified. Discuss these items during a meeting with the user and fill out a [[:File:Responsibility distribution.docx|'''responsibility table''']].
-Make sure that the designated responsible party is qualified to do so. “Neither the researchers, inclusively the PI's are in a place to take responsibility for work with technologies that they do not understand.”
+Make sure that the designated responsible party is qualified to do so. One respondent of our survey pointed out: “Neither the researchers, inclusively the PI's are in a place to take responsibility for work with technologies that they do not understand.”

← Older revision		Revision as of 08:32, 21 January 2021
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−	Give the users documents that he should read and sign.	+	Give the users documents that they should read and sign.

	== Rules, guidelines ==		== Rules, guidelines ==

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 == Rules, guidelines ==
-State the rules of the facility, give guidelines. Explain about CF procedures, communication, safety, pricing. Give information about [[Data management: Recommendations|data management]] (data naming convention, data saving, data transfer, data long-term storage)
+State the rules of the facility, give guidelines. Explain about CF procedures, communication, safety, pricing. Give information about [[Data management: Recommendations|'''data management''']] (data naming convention, data saving, data transfer, data long-term storage)
 Also state the duties of the users.

@@ Line 8: / Line 8: @@
 == Responsibilities ==
-Define responsibilities precisely. Who will be responsible (the CF, the user, the PI or another scientist) regarding the experimental design, sample preparation, data acquisition, data storage, data analysis, documentation and publication? The ones who carry the responsibility for doing or supervising/checking each step must be clearly defined before starting any experiments (as well as shared responsibilities). This will prevent that suboptimal results/procedure are not identified and go on as if they were fine. Discuss it all together at a meeting and fill up a responsibility table. [[File:Responsibility distribution.docx ]]
+Define responsibilities precisely. Who will be responsible (the CF, the user, the PI or another scientist) regarding the experimental design, sample preparation, data acquisition, data storage, data analysis, documentation and publication? The ones who carry the responsibility for doing or supervising/checking each step must be clearly defined before starting any experiments (as well as shared responsibilities). This will prevent that suboptimal results/procedure are not identified and go on as if they were fine. Discuss it all together at a meeting and fill up a [[:File:Responsibility distribution.docx|responsibility table]].
 Make sure that the designated responsible party is qualified to do so. “Neither the researchers, inclusively the PI's are in a place to take responsibility for work with technologies that they do not understand.”