Résultats de la recherche - 565 results
A validated ultra high pressure liquid chromatographic method for qualification and quantification of folic acid in pharmaceutical preparations.
A fully validated UHPLC method for the identification and quantification of folic acid in pharmaceutical preparations was developed. The starting conditions for the development were calculated starting from ...
Diagnostic performance and application of two commercial cell viability assays in foot-and-mouth disease research.
Abstract: Cell-based assays are still used widely in foot-and-mouth disease (FMD) research, despite the existence of a wide variety of molecular techniques. The aim of this study was to validate an automated, ...
Rapid analysis of melamine residue in milk, milk products, bakery goods and flour by ultra-performance liquid chromatography/tandem mass spectrometry: From food crisis to accreditation
chromatographic (UPLC) method with tandem mass spectrometry has been developed and validated for the determination of melamine in milk, milk products, bakery goods, and flour. The method comprises a simple ...
Influence of the incubation temperature and the batch components on the sensitivity of an enzyme-linked immunosorbent assay to detect Aujeszky's disease virus glycoprotein E (gE).
validated using the quality system criteria, even when all technical parameters were controlled. Incubation at different temperatures and batch composition were identified as parameters that could result in ...
Oral fluid for the serological and molecular diagnosis of measles.
validate the detection of anti-measles IgM and measles virus RNA in oral fluid and to make a comparison with the gold standard methods of ELISA using serum (Enzygnost(®) anti-Measles IgM) and in-house nested ...
Implementation over the past 20 years of the 3R's principle for batch release at the Scientific Institute of Public Health, Belgium (IPH).
Tetanus time toxicity use vaccine vaccines VALIDATION Validation study Weight Weight gain Weight-gain world Abstract: For the batch release of vaccines on the European market, a limited number of quality ...
A duplex real-time RT-PCR for the detection of bluetongue virus in bovine semen.
https://www.sciensano.be/en/biblio/a-duplex-real-time-rt-pcr-detection-bluetongue-virus-bovine-semen
(BTV). The aim of this study was to validate a real-time RT- PCR for the direct testing of semen for artificial insemination (AI). The amplification of the BTV target was combined with an internal control ...
Rapid method for the confirmatory analysis of chrysoidine in aquaculture products by ultra-performance liquid chromatography-tandem mass spectrometry.
than the only previously published method with gas chromatographic detection. A complete validation according to the scientific literature and as defined by the European Union was performed. The ...
Confidence in indirect assessment of foot-and-mouth disease vaccine potency and vaccine matching carried out by liquid phase ELISA and virus neutralization tests.
phase blocking competitive ELISA (lpELISA) and virus neutralization (VNT) in 10 potency trials using the same A24 Cruzeiro vaccine, were interpolated into previously validated logit transformation curves ...
Promotion of an applied pharmacokinetic software, named pharmonitor, developed to optimize individual dosage regimen through a national quality control program
customized according to the user’s selection (language, concentration units, drug target ranges, creatinine clearance, …). Reports can be generated in PDF format after appropriate validation. The software can ...