Results for studierapport translation from Danish to English

endelig studierapport
final study report

endelig studierapport:
final clinical study report:

endelige kliniske studierapport:
final clinical

data fra den kliniske studierapport
data from clinical study report

endelig klinisk studierapport q4 2017
final clinical study report q4 2017

endelig studierapport 31. december 2020
final study report by 31 december 2020

den kliniske studierapport skal indsendes inden
the clinical study report should be submitted by

afsluttende studierapport inden 15. december 2020
final study report by 15 december 2020

indsendelse af endelig studierapport: november 2019
final study report submission: november 2019

den endelige kliniske studierapport skal indsendes senest:
the final clinical study report should be submitted by:

en studierapport vil blive indsendt i slutningen af 2007.
a study report will be submitted by the end of 2007.

indsendelse af endelig studierapport: anden halvdel af 2018
final study report submission: 31

den endelige studierapport skal indsendes senest 31. marts 2017
the final clinical study report should be submitted by 31st march 2017

gennemgås hvert år endelig studierapport forventes klar senest q4 2008
to be reviewed annually final study report expected by 4q 2008

den endelige studierapport vil blive fremsendt til chmp, når denne er afsluttet.
the final study report will be provided to the chmp upon completion.

efter godkendelse af protokollen skal årlige rapporter fra dette studie indsendes sammen med psur´en indtil indsendelse af den endelige studierapport med frist december 2017.
after approval of the protocol, annual reports from this study shall be provided within the psur until submission of the final study report, which is due by december 2017.

indehaveren af markedsføringstilladelsen skal indsende den endelige studierapport til chmp og vurdere, om der er behov for at indsende en variation til produktresumeet vedrørende eventuelle signifikante resultater fremskaffet fra dette studium.
the mah should submit the final study report to the chmp and consider the need for a submission of a variation to the smpc for any significant results arising from this study.

indehaveren af markedsføringstilladelsen skal efter 1 år fremsende en studierapport med data fra et stort randomiseret, dobbeltblindet, placebokontrolleret sikkerhedsstudie baseret på en protokol, der er godkendt af chmp.
the mah shall provide the 1 year data report on a randomized, double-blind placebo- controlled large safety study, based on a protocol agreed with chmp.

pi tidligere ubehandlede (%) median baseline hiv- 1 rna, log10 kopier/ ml (iqr) median baseline cd4+ celletal, celler/ mm3 (iqr) data fra den kliniske studierapport
male race (white/black/asian)% age, median, yrs cdc category c (%) antiretroviral naïve (%) pi naïve (%) median baseline hiv-1 rna, log10 copies/ml (iqr) median baseline cd4+ cell count, cells/mm3 (iqr) data from clinical study report