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1920 – Effect of Tannic Acid on Strength of Concrete ; 1921 – Quantities of Materials for Concrete, D. A. Abrams en Stanton Walker (Recipes for concrete reporting its strength after 28 days of curing ranging from 2000 to 4000 psi). 1922 – Flexural Strength of Plain Concrete (Relationship between flexural strength and compressive strength)
CLSM consists of a mixture of Portland cement, water, aggregate and sometimes fly ash. Unlike ordinary concrete, CLSM has much lower strength. The strength of CLSM is less than 1,200 pounds per square inch (8.3 MPa), while ordinary concrete has strengths exceeding 3,000 pounds per square inch (21 MPa) [citation needed]. As a result, CLSM is not ...
The limits for nitrosamines in medicines have been set using internationally agreed standards (ICH M7(R1)) based on lifetime exposure. [12] Generally, people should not be exposed to a lifetime risk of cancer exceeding 1 in 100,000 from nitrosamines in their medicines. [ 12 ]
With regards to structure, the C 2 N 2 O core of nitrosamines is planar, as established by X-ray crystallography. The N-N and N-O distances are 132 and 126 pm, respectively in dimethylnitrosamine, [13] one of the simplest members of a large class of N-nitrosamines Nitrosamines are not directly carcinogenic.
The CTD is maintained by the International Council on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH). [ 1 ] [ 2 ] After the United States, European Union and Japan, the CTD was adopted by several other countries including Canada [ 3 ] and Switzerland.
In the 1980s, the European Union began harmonising regulatory requirements. In 1989, Europe, Japan, and the United States began creating plans for harmonisation. The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) was created in April 1990 at a meeting in Brussels.
N-Nitrosoglyphosate is the nitrosamine degradation product and synthetic impurity of glyphosate herbicide. The US EPA limits N-nitrosoglyphosate impurity to a maximum of 1 ppm in glyphosate formulated products. [1] N-Nitrosoglyphosate can also form from the reaction of nitrates and glyphosate.
The minimum essential documents that are required for the registration of pharmaceutical products designed for human use are specified in the document 'ICH Good Clinical Practices,' published in 1997 by the ICH [2] Example ICH essential documents that would be required in any US, EU or Japan based clinical trial would include: signed protocol ...