Sentence examples for expedite reporting from inspiring English sources

Exact(2)

A fairly recent HMIS development is the use of the internet to expedite reporting from districts (or health facilities) to the national level, such as the District Health Information System DHISS) which is now used by more than 30 countries.

Toxicities were also measured by recording the incidence and grading of adverse events (AEs) and serious AEs (SAEs; the study protocol extended the definition of an SAE to include any grade 4 laboratory abnormality in order to expedite reporting of grade 4 neutropenia).

Similar(58)

Only suspected unexpected serious adverse reactions (SUSARs) require expedited reporting to the MHRA.

SUSARs will be reported according to the relevant timelines; expected side effects will be reported in the annual safety report unless serious enough to warrant expedited reporting.

Whilst any suspected, unexpected, serious adverse reaction (SUSAR) involving insulin therapy will be reported according to the timelines for SUSARs, expected side effects of insulin will be reported in the annual safety report unless serious enough to warrant expedited reporting.

Any AE that is assessed as serious, is suspected of having a causal relationship to the trial medication and is unexpected is a SUSAR and will require expedited reporting to the MHRA/Ethics Committee as detailed below.

Expedited reporting to trial coordinators (trials unit and chief investigator) of some or all expected SAEs could serve as a useful early warning mechanism for unexpected rates of known SAEs.

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.

Expedited reporting will be carried out according to the local regulations.

Any adverse events which require expedited reporting will follow the system outlined below.

Better toxicity and adverse event reporting can be achieved by carefully considering what information is not urgently required and can be requested on the CRFs, and what information requires the expedited reporting mechanism used for SAEs.

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