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Laboratory Document Articles & Analysis
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In the observational study conducted from October 2019 through April 2021, 19 patients (4 patients from Qatar and 15 patients from French Guiana) were treated with L-glutamine (Endari) (0.3mg/kg), twice daily. Clinical and laboratory parameters were documented for the year prior to treatment initiation as baseline values and collected at 24, 48, and 72 weeks from ...
HORIBA’s newly developed data preparation tool allows users to extensively display and document the interplay of different HORIBA ONE PLATFORM devices as well as to influence the processes with regard to quality control. ...
The Nimbus series offers readabilities from 0.1mg to 0.1g and capacities from 80g up to 22kg so there will be a model to suit all users from precise pharmaceutical laboratories to manufacturing sites or factories. Ideal for measuring samples, Nimbus offers speedy results for labs assessing multiple quantities in a short time. ...
Often times juggling multiple processes, lab documentation and even several spreadsheets can increase the threat of missing something and risking non-compliance, fines or even worse a contamination. ...
Those standards and of course the demand of the analysis reliability require a regular validation of the analysis systems used in pharmaceutical laboratories. The WinASPECT PLUS validation software for the UV/Vis spectrophotometer SPECORD® PLUS offers the user to perform a validation comfortably on his own or have it done by a service specialist. ...
Those standards and of course the demand of the analysis reliability require a regular validation of the analysis systems used in pharmaceutical laboratories. The WinASPECT PLUS validation software for the UV/Vis spectrophotometer SPECORD PLUS offers the user to perform a validation comfortably on his own or have it done by a service specialist. ...
In addition, EPA alleged that Zep Inc., gave false certifications of compliance with FIFRA Good Laboratory Practices (GLP) on documents associated with the registration of three pesticides in its line of Enforcer brand insecticides - Enforcer RoachMax Bait, Enforcer AntMax Bait and Enforcer Fire Ant Bait. ...
In addition, EPA alleges that Zep gave false certifications of compliance with FIFRA Good Laboratory Practices (GLP) on documents associated with the registration of three pesticides in its line of Enforcer brand insecticides - Enforcer RoachMax Bait, Enforcer AntMax Bait and Enforcer Fire Ant Bait. ...
Separately, Chevron is trying to obstruct the release of documents in its “fraud” case in New York federal court before Judge Lewis A. ...
Recently, the New Jersey Department of Environmental Protection (NJDEP) announced that they had finalized the Vapor Intrusion Technical Guidance document. The guide was designed to provide assistance in the evaluation of contaminated sites. ...
This specification defines the minimum requirements for inspection agency personnel or testing agency laboratory personnel, or both, and the minimum technical requirements for equipment and procedures utilized in the testing and inspection of construction and materials used in construction. ...
Demonstration and documentation by a laboratory that there was judicious selection and control of organization, facilities, resources, and operations will enhance the credibility of the data produced and promote its acceptance. 1. Scope 1.1 This guide provides information on consensus good ...
Demonstration and documentation by a laboratory that there was judicious selection and control of organization, facilities, resources, and operations will enhance the credibility of the data produced and promote its ...
This practice facilitates comparisons of inter laboratory data from methods and field investigative studies. 1. Scope 1.1 This practice covers quantitative methods for the personal sampling and determination of bacterial endotoxin concentrations in poly-disperse metalworking fluid aerosols in workplace atmospheres. Users should have fundamental ...
Demonstration and documentation by a laboratory that there was judicious selection and control of organization, facilities, resources, and operations will enhance the credibility of the data produced and promote its acceptance. 1. Scope 1.1 This guide provides information on consensus good laboratory practices for ...
This specification covers the design and dimensional requirements for four types (Types I, II, III, and IV) of disposable bacteriological (Pasteur-type) nonvolumetric glass pipets suitable for replicate dispensing of drops of solutions and suspensions for laboratory purposes. The pipets shall be made of good quality, clear glass of either ...
This specification provides standard dimensional requirements for glass separatory funnels for general laboratory use. Separatory funnels shall be in the following types: Type 1A; Type 1B; Type 1C; Type 2; Type 3; and Type 4. ...
This specification covers the glasses commonly used to manufacture laboratory glass apparatus. Three types of glasses are included: Type I, Class A which is a low-expansion borosilicate glass, Type I, Class B which is an alumino-borosilicate glass, and Type II which is a soda-lime glass. ...
This specification covers platinum evaporating dishes suitable for water analysis and laboratory use. Platinum evaporating dishes shall be of the following types and capacities: Type I; Type II; and Type III. ...
This specification covers two types of metal ignition crucibles, nickel or platinum, complete with covers, for laboratory use. Two types of crucibles shall be classified according to their capacities: Type I is nickel with capacities of 100 mL and 250 mL and Type II is platinum with capacity of 20 mL. ...