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This assay is required for regulatory reporting in Canada (Health Canada, 2000).
In recent years, the Neutral Red Uptake assay (adapted from INVITTOX, 1990) has mostly been used to assess cytotoxic potential, and it is required for regulatory reporting purposes in Canada (Health Canada, 2000).
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Clinical writing, especially for regulatory reports, follows strict guidelines set up by organizations such as the U.S. Food and Drug Administration and the International Conference on Harmonisation.
These widespread price discrepancies, including those for oxygen services, have been noted in dozens of regulatory reports.
Employing graphical workflows interactively allows analysis in a team-based setting and facilitates identification of the most suitable graphics for publishing and regulatory reporting.
A systematic workflow, including predefined graphical templates, starting from the eDISH plot and including a series of line plots, scatter plots, box-plots, and Kaplan Meier plots helps to ensure completeness of evaluations, supports hypothesis generation and testing, and facilitates identification of the most suitable graphics for publishing and regulatory reporting.
This type of issue may occur in other applications (e.g. financial); for example, Takeuchi et al. (2006) mention that "For risk management and regulatory reporting purposes, a bank may need to estimate a lower bound on the changes in the value of its portfolio which will hold with high probability".
The regulatory reporting requirements for such funds should require reporting, on a confidential basis, information necessary to assess whether the fund or fund family is so large or highly leveraged that it poses a threat to financial stability.
However, company management would no longer have to be concerned about the stock price, shareholder value, and meeting regulatory reporting requirements for publicly traded companies.
While individual causality assessments made by staff during a trial allow for clinical decisions and adherence to regulatory reporting timelines, a central tenet is that evidence for causality is determined for registration purposes on the basis of aggregated data at the end of a trial or on meta-analysis with data from similar trials.
The legislation would keep in place the timeline for issuing final rules for definitions such as swaps and swap dealers, and for rules requiring record retention and regulatory reporting.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com