Search results - 13 results

Discrepancies between validated GC‐FID and UHPLC‐DAD methods for the analysis of Δ‐9‐THC and CBD in dried hemp flowers

https://doi.org/10.1002/dta.3354 File:  Version:  Published Full text access:  Restricted Access Full text language:  English Category:  A1 FOS Classification:  3.05 Other medical sciences ...

Comparative Evaluation of Lumpy Skin Disease Virus-Based Live Attenuated Vaccines.

Balkans against lumpy skin disease virus (LSDV) was successful and has been implemented with success in the past in other countries, data of vaccine failure have also been reported. It was therefore the ...

CBD oils on the Belgian market: A validated MRM GC-MS/MS method for routine quality control using QuEChERS sample clean up

content by a CBN standard and the screening of seven other cannabinoids namely CBN, CBDV, CBT, CBC, Δ8- THC, THCV and CBG. The method was validated at three concentration levels (0.5–1–2% (w/v)) for CBD and ...

Deepening of In Silico Evaluation of SARS-CoV-2 Detection RT-qPCR Assays in the Context of New Variants

and January 2021. The lower inclusivity of the China CDC assay targeting the gene N has continued to decrease with new mismatches detected, whereas the other evaluated assays kept their inclusivity ...

Use of Whole Genome Sequencing Data for a First in Silico Specificity Evaluation of the RT-qPCR Assays Used for SARS-CoV-2 Detection.

human reference genome and 2624 closely related other respiratory viral genomes. The specificity of the assays was generally good and stable over time. An exception is the first method developed by the ...

Analytical validation of tests in laboratories of anatomic pathology: a Belgian population-based study

van de medische laboratoria Manuscript versions:  File:  Version:  Published Full text access:  Public Access Full text language:  English Category:  A1 FOS Classification:  3.05 Other medical sciences ...

Analysis of illegal peptide drugs via HILIC-DAD-MS.

been developed to detect and quantify these peptides. The emerging of more polar peptides however requires the introduction of other separation techniques. Therefore, we set out to develop and validate ...

A new approach to define acceptance limits for hematology in external quality assessment schemes.

CONCLUSIONS: The approach enabled to determine state of the art-based AL s, that were concentration-dependent when necessary and usable by various EQA providers. It could also easily be applied to other ...

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