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3421“…BACKGROUND: Reporting of adverse drug reactions (ADRs) has traditionally been the sole province of healthcare professionals. In the European Union, more countries have allowed consumers to report ADRs directly to the regulatory agencies. …”
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3422por Valadez, Joseph J., Berendes, Sima, Jeffery, Caroline, Thomson, Joanna, Ben Othman, Hussain, Danon, Leon, Turki, Abdullah A., Saffialden, Rabea, Mirzoyan, Lusine“…The dispute resolution in 2003 included an agreement with the European Union on humanitarian cooperation and the development of Libya’s first National HIV Strategy. …”
Publicado 2013
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3423por Dorresteijn, Ine, Hartel, Tibor, Hanspach, Jan, von Wehrden, Henrik, Fischer, Joern“…Given the apparent habitat value of wood pastures for woodpeckers we recommend wood pastures be explicitly considered in relevant policies of the European Union, namely the Habitats Directive and the EU Common Agricultural Policy.…”
Publicado 2013
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3424“…MATERIALS AND METHODS: The data of clinical trials registered in India, United States (US), and European Union (EU) were obtained from websites of CTRI, clinicaltrial.gov and EU clinical trial registry, respectively from July 20, 2007 to August 29, 2011 for a period of 4 years. …”
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3425“…CONCLUSIONS: The existing QA guidance for mammography is derived from key documents (American College of Radiology and European Union guidelines) and proposes similar tests despite the variations in detail and methodologies. …”
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3426“…The immune response against B antigen met the European Union Licensure criteria regarding the geometric mean titer ratio in the MF group (2.4), but not in the placebo group (1.7). …”
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3427“…METHODS: Data were obtained from a literature review, a Master thesis in Pharmaceutical Care at the Catholic University of Leuven and a mailing sent to all members of the Pharmaceutical Group of the European Union with a request for information about the local remuneration systems of community pharmacists and the possible existence of reports on discounting practices. …”
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3428“…The three main reasons were the high costs for proper implementation, the subjective value assigned to the reprocessing unit in health care facilities, and deficits in monitoring by the health authority. Throughout the European Union, a similar regulatory framework for the performance of the reprocessing process exists, while the environment, structures of the health systems and administrative supervision vary significantly. …”
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3429A framework to start the debate on neonatal screening policies in the EU: an Expert Opinion Documentpor Cornel, Martina C, Rigter, Tessel, Weinreich, Stephanie S, Burgard, Peter, Hoffmann, Georg F, Lindner, Martin, Gerard Loeber, J, Rupp, Kathrin, Taruscio, Domenica, Vittozzi, Luciano“…The European Union (EU) Council Recommendation on rare diseases urged the member states to implement national and EU collaborative actions to improve the health care of rare disease patients. …”
Publicado 2014
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3430por Alvarez-del Arco, Debora, Monge, Susana, Caro-Murillo, Ana M., Ramírez-Rubio, Oriana, Azcoaga-Lorenzo, Amaya, Belza, Maria J., Rivero-Montesdeoca, Yaiza, Noori, Teymur, Del Amo, Julia“…Background: In the context of an European Centre for Disease Prevention and Control (ECDC) research project, our objective was to describe current recommendations regarding HIV testing and counselling targeting migrants and ethnic minorities in the European Union/European Economic Area/European Free Trade Association (EU/EEA/EFTA) Member States. …”
Publicado 2014
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3431“…BACKGROUND: Microbiological standards within pork slaughter processing plants in the European Union are currently governed by Commission Regulation (EC) 2073/2005, which describes detailed performance criteria at specific stages of the procedure (following carcass dressing and before chilling) for total viable counts (TVC), Enterobacteriaceae (EB) and Salmonella spp. …”
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3432“…BACKGROUND: The majority of fatalities on the European Union (EU) railways are suicides, representing about 60% of all railway fatalities. …”
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3433“…A DMF analog, BG-12, was recently approved for the treatment of relapsing-remitting MS by the European Union and the US Food and Drug Administration. …”
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3434por Knight-Jones, T.J.D., Bulut, A.N., Gubbins, S., Stärk, K.D.C., Pfeiffer, D.U., Sumption, K.J., Paton, D.J.“…The arrival of the FMD Asia-1 serotype in Turkey in 2011 caused particular concern, spreading rapidly westwards across the country towards the FMD free European Union. With no prior natural immunity, control of spread would rely heavily on vaccination. …”
Publicado 2014
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3435por Stoffer, Michaela A, Smolen, Josef S, Woolf, Anthony, Ambrozic, Ales, Bosworth, Ailsa, Carmona, Loreto, Fialka-Moser, Veronika, Loza, Estibaliz, Olejnik, Pawel, Petersson, Ingemar F, Uhlig, Till, Stamm, Tanja A“…OBJECTIVE: The eumusc.net project is a European Union (EU) commission and European League Against Rheumatism (EULAR)funded project that aims to facilitate equal standards for musculoskeletal health in all EU countries. …”
Publicado 2014
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3436por Oomen, Agnes G., Bos, Peter M. J., Fernandes, Teresa F., Hund-Rinke, Kerstin, Boraschi, Diana, Byrne, Hugh J., Aschberger, Karin, Gottardo, Stefania, von der Kammer, Frank, Kühnel, Dana, Hristozov, Danail, Marcomini, Antonio, Migliore, Lucia, Scott-Fordsmand, Janeck, Wick, Peter, Landsiedel, Robert“…Bringing together topic-related European Union (EU)-funded projects, the so-called “NanoSafety Cluster” aims at identifying key areas for further research on risk assessment procedures for nanomaterials (NM). …”
Publicado 2014
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3437por Katelaris, Constance H., Kurosawa, Motohiro, Moon, Hee-Bom, Borres, Magnus, Florvaag, Erik, Johansson, Stig Gunnar Olof“…Nevertheless, the European Medicines Agency in 2011 advised to continue the unrestricted use throughout the European Union. OBJECTIVE: To extend studies on PHO consumption and prevalence of IgE-sensitization to morphine (MOR), PHO, and SUX to countries representing high (Australia), and low (Korea and Japan), consumers, respectively. …”
Publicado 2014
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3438por Meller, Stephanie M, Baumbach, Andreas, Voros, Szilard, Mullen, Michael, Lansky, Alexandra J“…Consensus from the 2013 Yale-UCL Device Innovation Summit specifically recommends the reporting of mean single lesion volume, number of new lesions, and total volume, and encourages European Union (EU)-US regulatory consensus in the guidance of implementing this endpoint.…”
Publicado 2013
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3439por Helyar, Sarah J., Lloyd, Hywel ap D., de Bruyn, Mark, Leake, Jonathan, Bennett, Niall, Carvalho, Gary R.“…Initiatives encompass new legislation in the European Union requiring the inclusion of species names on catch labels throughout the distribution chain. …”
Publicado 2014
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3440“…This is given special attention in the European Union (EU) efforts to minimize human food-borne Salmonella infections from animal-derived food. …”
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