EQIPD (European Quality in Preclinical Data)is a consortium promoting robustness, rigor and validity in preclinical research. Members of the consortium have produced substantial evidence which suggests that the robustness, rigour and validity of preclinical research is limited and that this provides a barrier to the effective and efficient development of new drugs. EQIPD believes there is a need for simple, sustainable solutions that facilitate data quality without impacting innovation and freedom of research.
The project pools resources from both academia and industry to pilot this action in Neuroscience and Safety, facilitated by analysis of historical datasets held by EFPIA consortium members data management system developed for the Systematic Review & Meta-analysis Facility (SyRF).
The Quality System, constructed as a wiki, can be accessed here.
Malcolm Macleod has recorded three video presentations of EQIPD (Why, What and How): Part 1 provides the background on why the EQIPD quality system is needed and for whom it is important. He also talks about the benefit of implementing such a system in any research lab. Part 2 introduces the Core Requirements and the four key guiding principles when designing the quality system: flexible, fit-for-purpose, lean and user-friendly. Part 3 explains the steps that can be taken to implement the quality system.
Fant du det du lette etter?Ja, jeg fant det! Nei, jeg fant det ikke!
Takk for din tilbakemelding! Vær oppmerksom på at vi ikke kan kontakte deg hvis ikke du oppgir din epostadresse.
Hva lette du etter?
Gi oss gjerne en tilbakemelding slik at vi kan forbedre informasjonen på siden. På forhånd takk for hjelpen! Vennligst skriv inn din epostadresse hvis du vil ha et svar.Kontakt oss gjerne på e-post hvis du har spørsmål.