Risks of emergency use authorizations for medical products during outbreak situations: a COVID-19 case study

Abstract Background The world is facing an unprecedented outbreak affecting all aspects of human lives which is caused by the COVID-19 pandemic. Due to the virus novelty, healthcare systems are challenged by a high rate of patients and the shortage of medical products. To address an increased need f...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Almir Badnjević, Lejla Gurbeta Pokvić, Zijad Džemić, Fahir Bečić
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BMC 2020-10-01
Sarja:BioMedical Engineering OnLine
Aiheet:
Medical device
Outbreak
COVID-19
Regulatory framework
Import
Market placement
Linkit:http://link.springer.com/article/10.1186/s12938-020-00820-0
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