Clinical Ethics Concerns of Rural Healthcare Providers
Journal of Regional Medical Campuses, 2023 Purpose: This project aimed to identify ethical concerns in rural hospitals and elicit ideas for establishing clinical ethics services to meet needs.
Catherine McCarty +2 more
doaj +1 more source
Canada’s new ethical guidelines for research with humans: A critique and comparison with the United States [PDF]
, 2012 Canada’s Tri-Council Policy Statement: Ethical conduct for research involving humans, first published in 1998, has recently been updated.1 The US Department of Health and Human Services has just issued an Advance Notice of Proposed Rulemaking that would ...
Millum, J.
core +1 more source
Safety and efficacy of colistin versus meropenem in the empirical treatment of ventilator-associated pneumonia as part of a macro-project funded by the Seventh Framework Program of the European Commission studying off-patent antibiotics. study protocol for a randomized controlled trial [PDF]
, 2015 Background: Ventilator-associated pneumonia (VAP) is one of the most common and severe hospital-adquired infections, and multidrugresistant gram-negative bacilli (MDR-GNB) constitute the main etiology in many countries.
Clara Rosso, Fernández +6 more
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Access to Ethics Committees in Bulgaria – Possibility or Probability
Acta Medica Bulgarica, 2019 The study of the legal framework regulating the activities of the Ethics Committees in the Member States of the European Union outlines several key factors forming the basis of the activity of the Ethics Committees. Compliance with the ethical principles
Gradinarova N.
doaj +1 more source
Ethics committees in India: Facing the challenges!
Perspectives in Clinical Research, 2012 The past few years have seen a tremendous rise in the number of clinical trials conducted in India. This is been attributed to the huge patient population, genetic diversity, and rich technical pool in our country.
Rashmi Kadam, Shashikant Karandikar
doaj +1 more source
Informed consent in clinical research; Do patients understand what they have signed? [PDF]
Farmacia Hospitalaria, 2016 Informed consent is an essential element of research, and signing this document is required to conduct most clinical trials. Its aim is to inform patients what their participation in the study will involve.
Elena Villamañán +7 more
doaj +1 more source
Ethics, space, and somatic sensibilities: comparing relationships between scientific researchers and their human and animal experimental subjects [PDF]
, 2011 Drawing on geographies of affect and nature-society relations, we propose a radical rethinking of how scientists, social scientists, and regulatory agencies conceptualise human and animal participants in scientif ic research. The scientific rationale for
Birke L +33 more
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Research ethics committees in Latin America: What do they accomplish?
Revista Colombiana de Bioética, 2019 The outsourcing of clinical trials to Latin America began in the mid-1940s under the sponsorship of universities and the National Institutes of Health of the United States of America.
Antonio Ugalde, Nuria Homedes
doaj +1 more source
Clinical ethics protocols in the clinical ethics committees of Madrid
Journal of Medical Ethics, 2013 Currently, The nature and scope of Clinical Ethics Protocols (CEPs) in Madrid (Spain) are not well understood.The main objective is to describe the features of 'guideline/recommendation' type CEPs that have been or are being developed by existing Clinical Ethics Committees (CECs) in Madrid.
Herreros Ruiz Valdepeñas, Benjamín +5 more
openaire +4 more sources
Design of a prospective observational study on the effectiveness and real-world usage of recombinant factor VIII Fc (rFVIIIFc) compared with conventional products in haemophilia A: The A-SURE study [PDF]
, 2019 Introduction: Haemophilia A is a rare bleeding disorder caused by coagulation factor VIII (FVIII) deficiency. This is treated with factor VIII, conventionally using products with a half-life of 8-12 hours typically administered every 2-3 days ...
Hay, Charles R.M. +7 more
core +3 more sources