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Although consideration of chemical mixtures is not new to either realm, there is currently, and has been for the past decade, a greater emphasis on development of both scientific and regulatory methodology to improve our ability to evaluate the human and environmental health impacts of chemical mixtures (although only human health was addressed here).
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We further conclude that during 23 years of EU regulation for GM organisms and various GM crop risk assessments and approvals, regulatory sciences and methodology are used that were developed under the contrasting US regulatory concept.
One of these tools is a building regulatory capacity assessment methodology to assess and document building regulatory practices in low and middle-income countries.
However, an examination of the time to the first postmarket regulatory warning, the methodology that was used in this paper, is consistent with what other authors have carried out in analysing the postmarket safety profile of drugs in general, 16 specific classes of drugs 15 and in comparing different groups of drugs.
Because researchers and regulators working to improve the human health assessment of chemical mixtures will likely build upon past regulatory and toxicologic methodology and technology, it is relevant to consider the past century of toxicology and chemical regulation and consider past goals and limitations in both the science and regulation of chemicals.
Furthermore, the Guidance offers a good opportunity to the pharmaceutical industry to discuss about methodology with regulatory authorities, and to become a trustworthy partner of regulatory agencies.
A systematic methodology for regulatory control analysis and design is adapted for sewer system operation and evaluated.
When developing new methodology, new regulatory guidelines, or a new science, it may be useful to consider the forces acting to shape them (e.g., the existing knowledge base, available technology, funding, research opportunities, academic and government needs).
Because the legal and regulatory landscape surrounding sound methodologies and best practices is admittedly complicated and often unclear, one should identify and retain appropriate legal counsel and obtain necessary legal advice before conducting any Malware forensic investigation.
In this methodology, design and regulatory requirements for safety of nuclear power plants are considered simultaneously.
Means-end analysis, also called functional modelling, is proposed as a methodology to model regulatory networks.
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