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A serious adverse event that is sudden in its onset, unexpected in its severity and seriousness or not a known side effect of the IMP and related or suspected to be related to the IMP is classed as SUSAR and requires expedited reporting as per the clinical trials regulations.
The OPU/DMR can be configured for periodic- or event-based reporting as per the measurement control command provided.
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Chemical shifts are reported as per million (δ ppm) using tetramethylsilane (TMS) as internal standard or by reference to proton resonances resulting from incomplete deuteration of the NMR solvent.
All ChIP-seq data are normalized by library depth and reported as per million mapped reads (RPM).
Stable isotope results are reported as per mil deviations from the VPDB and AIR reference standard scale for δ 13C and δ 15N values, respectively.
The 18O/16O ratio of the CO2(g) was then measured on a Micromass MS903 mass spectrometer and the δ18O reported as per mil deviation from the Vienna Standard Mean Ocean Water (VSMOW) using the delta -scale with measurement accuracy of ±0.15.
Results were reported as per the Richart CIN staging system in five categories of increasing disease severity: normal/no neoplastic abnormalities, CIN1, CIN2, CIN3, and invasive cervical cancer (ICC).
All experiments are accurately reported as per ARRIVE guidelines.
Cytology will be reported as per the Australian Modified Bethesda System [ 37].
Smear results were reported as per WHO/IUATLD classification [ 15].
Office visits and patient-initiated phone calls were reported as per member per year rates.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com