Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Más filtros

Banco de datos
Tipo del documento
Publication year range
1.
Bioanalysis ; 16(11): 505-517, 2024 Jun 02.
Artículo en Inglés | MEDLINE | ID: mdl-38864397

RESUMEN

The 16th GCC Closed Forum was held in Orlando, FL, USA, on 23 June 2023. Representatives from international bioanalytical Contract Research Organizations were in attendance in order to discuss scientific and regulatory issues specific to bioanalysis. The issues discussed at the meeting included: IS response, flow cytometry, changes to the bioanalytical industry, NGS assays, biomarker assay for tissues, dPCR validation, immunogenicity harmonization and ICH M10 implementation. Conclusions and consensus from discussions of these topics are included in this article.


Asunto(s)
Biomarcadores , Citometría de Flujo , Citometría de Flujo/normas , Citometría de Flujo/métodos , Biomarcadores/análisis , Humanos , Secuenciación de Nucleótidos de Alto Rendimiento , Reacción en Cadena en Tiempo Real de la Polimerasa/métodos
2.
Bioanalysis ; 14(12): 853-863, 2022 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-35703321

RESUMEN

Gene therapy, cell therapy and vaccine research have led to an increased use of qPCR/ddPCR in bioanalytical laboratories. CROs are progressively undertaking the development and validation of qPCR and ddPCR assays. Currently, however, there is limited regulatory guidance for the use of qPCR and a complete lack of any regulatory guidelines for the use of the newer ddPCR to support regulated bioanalysis. Hence, the Global CRO Council in Bioanalysis (GCC) has issued this White Paper to provide; 1) a consensus on the different validation parameters required to support qPCR/ddPCR assays; 2) a harmonized approach to their validation and 3) a consistent development of standard operating procedures (SOPs) for all the bioanalytical laboratories using these techniques.


Asunto(s)
Bioensayo , Reacción en Cadena en Tiempo Real de la Polimerasa/métodos
3.
Bioanalysis ; 14(4): 187-193, 2022 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-35135309

RESUMEN

Gene therapy, cell therapy and vaccine research have led to an increased need to perform cellular immunity testing in a regulated environment to ensure the safety and efficacy of these treatments. The most common method for the measurement of cellular immunity has been Enzyme-Linked Immunospot assays. However, there is a lack of regulatory guidance available discussing the recommendations for developing and validating these types of assays. Hence, the Global CRO Council has issued this white paper to provide a consensus on the different validation parameters required to support Enzyme-Linked Immunospot assays and a harmonized and consistent approach to Enzyme-Linked Immunospot validation among contract research organizations.


Asunto(s)
Bioensayo/métodos , Tratamiento Basado en Trasplante de Células y Tejidos/métodos , Ensayo de Immunospot Ligado a Enzimas/métodos , Terapia Genética/métodos , Humanos
SELECCIÓN DE REFERENCIAS
Detalles de la búsqueda