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Location of Cynological Units in the Structure of the National Police of Ukraine and in the System of the Ministry of the Internal Affairs
Published 2019-09-01“…For what was analyzed the current state of the legal framework that provides the activities of the canine units of the National Police of Ukraine (NPU), considered the historical features of the development of the canine service in the system of bodies subordinate to the Ministry of Internal Affairs (MIA). …”
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A Machine Learning Algorithm to Predict Medical Device Recall by the Food and Drug Administration
Published 2024-11-01“…Identification of dangerous medical devices as early as possible is necessary to minimize patient harms while avoiding false positives to prevent removal of safe devices from use. While the United States Food and Drug Administration (FDA) employs an adverse event reporting program (MedWatch) and database (MAUDE), other data sources and methods might have utility to identify potentially dangerous medical devices. …”
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Effects of anti-inflammatory drugs on fever and neutrophilia induced by Clostridium difficile toxin B
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Intravenous push administration of anti-seizure medications
Published 2025-01-01Get full text
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Important Things to Know about Medicare Chapter Five: Medicare Part D--Prescription Drug Coverage
Published 2014-02-01Get full text
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Important Things to Know about Medicare Chapter Five: Medicare Part D--Prescription Drug Coverage
Published 2014-02-01Get full text
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Requirements and special considerations for drug trials with children across six jurisdictions: 2. Ethics review in the regulatory approval process
Published 2025-02-01“…This work, undertaken by the Working Group (WG) on International Collaborations at the European Network of Pediatric Research at the European Medicines Agency (Enpr-EMA) aims to describe the research ethics review requirements including any pediatric specific requirements, as well as current or upcoming changes across six jurisdictions – the European Union (EU), United Kingdom (UK), United States of America (USA), Canada, Japan, and Australia.MethodsAn open questionnaire developed by the WG and directed at both the Competent Authorities (CA) and the national pediatric clinical trial networks arranged by jurisdictions.ResultsA synopsis of the current regulatory requirements covers centralized versus independent review, comparisons between investigator initiated and industry sponsored clinical trials, timelines, review board members requirements and the consenting/assent process for clinical trial (CT) applications, application submission processes and application requirements for each of the six jurisdictions. …”
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Possibility of using a mouse SCID as a model animal to variola virus for evaluating anti-smallpox drug efficacy
Published 2015-12-01“…This opens up the prospect of using SCID mice as an animal model for smallpox to develop antiviral drugs intended for people with severe immunosuppressive states.…”
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EGFR-Mutant Non-small Cell Lung Cancer: State-of-the-Art and Future Perspectives
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Linear IgA bullous dermatosis secondary to drugs: a real-world pharmacovigilance study of the FDA adverse event reporting system
Published 2025-01-01“…The gender distribution of reports was relatively balanced, with the highest proportion in the 66–85 age group. The United States had the highest number of reports. Vancomycin and Amoxicillin were the most frequently reported drugs, with 559 and 58 reports, respectively. …”
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