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Availability and use of Standards in vaccine development.
Avumegah, Michael Selorm; Mattiuzzo, Giada; Särnefält, Anna; Page, Mark; Makar, Karen; Lathey, Janet; Kim, June; Yimer, Solomon Abebe; Craig, Danielle; Knezevic, Ivana; Bernasconi, Valentina; Kristiansen, Paul A; Kromann, Ingrid.
Afiliación
  • Avumegah MS; Coalition for Epidemic Preparedness Innovations (CEPI), Oslo, Norway. selorm.avumegah@cepi.net.
  • Mattiuzzo G; Medicines and Healthcare products Regulatory Agency (MHRA), Potters Bar, UK.
  • Särnefält A; Coalition for Epidemic Preparedness Innovations (CEPI), Oslo, Norway.
  • Page M; Medicines and Healthcare products Regulatory Agency (MHRA), Potters Bar, UK.
  • Makar K; Bill & Melinda Gates Foundation (BMGF), Seattle, USA.
  • Lathey J; National Institute of Allergy and Infectious Diseases (NIAID), Bethesda, USA.
  • Kim J; Coalition for Epidemic Preparedness Innovations (CEPI), Oslo, Norway.
  • Yimer SA; Coalition for Epidemic Preparedness Innovations (CEPI), Oslo, Norway.
  • Craig D; Coalition for Epidemic Preparedness Innovations (CEPI), Oslo, Norway.
  • Knezevic I; World Health Organization (WHO), Geneva, Switzerland.
  • Bernasconi V; Coalition for Epidemic Preparedness Innovations (CEPI), Oslo, Norway.
  • Kristiansen PA; Coalition for Epidemic Preparedness Innovations (CEPI), Oslo, Norway.
  • Kromann I; Coalition for Epidemic Preparedness Innovations (CEPI), Oslo, Norway.
NPJ Vaccines ; 8(1): 95, 2023 Jun 30.
Article en En | MEDLINE | ID: mdl-37391580
Reference materials are critical in assay development for calibrating and assessing their suitability. The devasting nature of the COVID-19 pandemic and subsequent proliferation of vaccine platforms and technologies has meant that there is even a greater need for standards for immunoassay development, which are critical to assess and compare vaccines' responses. Equally important are the standards needed to control the vaccine manufacturing processes. Standardized vaccine characterization assays throughout process development are essential for a successful Chemistry, Manufacturing and Controls (CMC) strategy. In this perspective paper, we advocate for reference material incorporation into assays and their calibration to International Standards from preclinical vaccine development through control testing and provide insight into why this is necessary. We also provide information on the availability of WHO international antibody standards for CEPI-priority pathogens.

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: NPJ Vaccines Año: 2023 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: NPJ Vaccines Año: 2023 Tipo del documento: Article