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elifesciences / elife-vendor-workflow-config

capturing requriemtns and niggles for setting up the elife production workflow
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<fn-group content-type="ethics-information"> Ethics information #72

Open Melissa37 opened 9 years ago

Melissa37 commented 9 years ago

This is a footnote group - ethics information This is not mandatory and depends whether the authors have included this information in their submission. It will be included in the xml output from the submission system.

This contains one/none/two or all three sections: Clinical trial registration Human subjects: Animal experimentation:

<fn-group content-type="ethics-information"><title>Ethics</title><fn fn-type="other"><p>Clinical trial registration CB7778886452342</p></fn><fn fn-type="other"><p>Human subjects: Blah blah blah</p></fn><fn fn-type="other"><p>Animal experimentation: Blah blah blah</p></fn></fn-group></sec>

Please do not edit the text, it is output as required form the submission system.

ghost commented 9 years ago

This is added in Bugzilla http://bugzilla.exetercs.com/show_bug.cgi?id=4001

Melissa37 commented 9 years ago

This has been amended. See commit https://github.com/elifesciences/elife-vendor-workflow-config/commit/fc5e502f2dac33e2c019accaa174f4d62a47a6ee and https://github.com/elifesciences/elife-vendor-workflow-config/commit/a1dd3bca7df95987470a2abc735417949f921f2f

Basically, any clinical trials should be added to the end of the abstract, as well as change the format in the ethics footnote.