Search results - 9 results

Belgian recommendations for analytical verification and validation of immunohistochemical tests in laboratories of anatomic pathology

analysis taking into account the majority of variables regarding verification/validation of methods have been performed, resulting in an expert consensus recommendation that is a compromise between ...

Surveillance of COVID-19 mortality in Belgium, epidemiology and methodology during 1st and 2nd wave (March 2020- 14 February 2021)

both for the total period and for the second wave. International comparison and ranking of COVID-19 crude mortality rates are misleading because of very heterogeneous methods used (e.g. case definition, ...

Dietary exposure to pyrrolizidine alkaloids in young children and adults from the Belgian population (PASFOOD)

developed at WIV- ISP for the analysis of 16 PA s and 14 PANO s. The sample preparation and instrumental methods were optimized to obtain the best method sensitivity. Nine analytical methods were validated ...

Method validation of nanomaterial characterization by single particle ICP-MS, DLS and quantitative TEM analyses. Final report NanoVAL.

Publication Type: Sci. report, recommendat°, guidance doc., directive, monograph Authors: Bozatzidis,V; Delfosse,L.; Annick Evrard; Nadia Waegeneers Source: CODA-CERVA, Brussels, Belgium, p.NA (2016) Accession Number: NA Keywords: DLS ICP-MS nanomaterials ...

The vaccines consistency approach project: an EPAA initiative

approaches at concept Control developing European European Commission Human improve Industries Industry Laboratories method methods Monitoring Order parameters PROCESSES production Project Quality Quality ...

Establishment of hepatitis A vaccine (inactivated, non-adsorbed) BRP batches 2 and 3

HAV (inactivated), using the standard in vitroELISA (enzyme-linked immunosorbent assay) method validated previously. The results of the study showed that the candidate BRP s were suitable for the ...

Validation of a new ELISA method for in vitro potency testing of hepatitis A vaccines

use vaccine vaccines Validate VALIDATION VIRUS Abstract: The goal of the project was to standardise a new in vitro method in replacement of the existing standard method for the determination of ...

Calibration of the Ph. Eur. Biological Reference Preparation (BRP) for Tetanus Vaccine (Adsorbed) Batch 3).

healthcare Impact Institute International International Standard interval IS IT Laboratories Medicine medicines method methods mice n observed ON organisation organization outcome PARTICIPANTS performance ph ...

Collaborative Study for the Validation of Alternative in vitro Potency Assays for Human Tetanus Immunoglobulin

vivo assay to be performed to determine the potency of human tetanus immunoglobulins during their development. Furthermore, it states that an in vitro method shall be validated for the batch potency ...

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