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But applying the open-source methodology to pharmaceutical consumers is a relatively new idea.
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Performing a CEA on a health promotion intervention, however, has some implications for the CEA methodology, compared to pharmaceutical interventions.
We present a methodology to evaluate the sensitivity of pharmaceutical batch processes to scaling up.
Forced degradation studies are used to facilitate the development of analytical methodology, to gain a better understanding of active pharmaceutical ingredient (API) and drug product (DP) stability, and to provide information about degradation pathways and degradation products.
This paper describes a case study using a cyclone-design methodology to increase cyclone collection efficiency for spray-dried dispersions (SDDs) for pharmaceutical applications.
It stimulates pharmaceutical companies to use a shared and accepted methodology to provide data, although an alternative approach is considered possible.
The approach of compositing biosolids was validated for pharmaceuticals and personal care products (PPCPs), BFRs, alkylphenol surfactants, and perfluorinated compounds (PFCs), which demonstrates this methodology to provide defensible national baseline levels of contaminants in U.S. biosolids.
"My principle of work is based on training and methodology: to have the right training methodology.
Develin then applied his methodology to the environment.
Where's the methodology to calculate a fair fine?
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com