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CR is currently available as a research tool in an open research environment containing various prototype software (Frontier, version 1.0.0, syngo.Via, version VB10A, Siemens Healthcare, Forchheim, Germany) and has so far no approval for clinical use.
TNFα has no approval for perfusion in the United States.
Further, local medical ethical committee requires no approval for retrospective studies.
This study was exempt from ethical review, and no approval for use of data was necessary, since it was based on a retrospective chart review and analyses were performed on an anonymized database.
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After virtually no approvals for several years, China granted permission last year for over half a dozen private power projects.
Consequently no approval from the Regional Committees for Medical and Health Research Ethics REKK) was necessary.
In Sweden there is no approval process for prescribing medicines with limited reimbursement provided within the PBS.
There is currently no governmental approval for UW, thus no UW solution available on the German market.
There was to be no playful wave to the crowd, no roared approval for the new man at the helm.
Danish legislation requires no ethical approval for this type of study (see Act on Research Ethics Review of Health Research Projects, Law no. 593, 14 June 2011; http://www.cvk.sum.dk/English/actonabiomedicalresearch.aspx).aspx
They voted that no formal approval for the quantitative approach is required since no direct patient contact is involved.
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CEO of Professional Science Editing for Scientists @ prosciediting.com