ASQ TR1-2012

ASQ TR1-2012

Best quality practices for biomedical research in drug development

63,00 €

Detalles

This Technical Report identifies important quality management system elements for non-regulated biomedical research in drug development in order to ensure credibility of biomedical research results. This includes both large and small molecule discovery and non-clinical development that is not covered by GxP.
The target audience for this report is the scientific staff at institutions and companies involved in drug development. Compliance with applicable regulatory and safety requirements is not covered by this report.

This Technical Report was created by a working group from the Food, Drug and Cosmetic Division of the American Society for Quality.

Información adicional

Autor American Society for Quality (ASQ)
Publicado por ASQ
Tipo de Documento Norma
Número de páginas 26
Palabra clave ASQ TR1-2012