Results 341 to 350 of about 1,261,156 (366)
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Serious Adverse Event Reporting in a Medical Device Information System
2011The paper describes the design of a module that manages Serious Adverse Events (SAEs) reporting within a Clinical investigation on Medical devices. This module is integrated in a Medical Device Information System (MEDIS) that collects data and documents exchanged between applicants and the National Competent Authority during the clinical investigation ...
Daniela Luzi, Fabrizio Pecoraro
openaire +3 more sources
The Vaccine Adverse Event Reporting System
Journal of Toxicology: Clinical Toxicology, 1998openaire +3 more sources
The need for a chiropractic adverse events reporting system in Australia
Medical Journal of Australia, 2014John E Cunningham+2 more
openaire +3 more sources
A review of cancer immunotherapy toxicity
Ca-A Cancer Journal for Clinicians, 2020Lucy Boyce Kennedy
exaly
Radiation therapy‐associated toxicity: Etiology, management, and prevention
Ca-A Cancer Journal for Clinicians, 2021Kyle Wang
exaly
International Immunopharmacology, 2021
Chen Chen, Bin Wu, Chenyu Zhang, Ting Xu
semanticscholar +1 more source
Chen Chen, Bin Wu, Chenyu Zhang, Ting Xu
semanticscholar +1 more source