Showing 5,141 - 5,160 results of 6,841 for search '"Japan"', query time: 0.10s Refine Results
  1. 5141

    Heinrich Coudenhove-Kalergi a Mitsuko Aoyama: cesty, prostor a čas na přelomu 19. a 20. století by Radmila Švaříčková Slabáková

    Published 2013-06-01
    “… The article explores travels and the ways of travelling of count Heinrich Coudenhove-Kalergi, father of the founder of pan-European movement Richard Coudenhove-Kalergi, and his wife Mitsuko Aoyama, focusing not only on their travel from Japan to Europe in 1896 but also on the necessity of their further travels in Europe, planned carefully by Heinrich, with the aim to educate Mitsuko. …”
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  2. 5142
  3. 5143

    Requirements and special considerations for drug trials with children across six jurisdictions: 2. Ethics review in the regulatory approval process by Breanne Stewart, Pirkko Lepola, Gunter F. Egger, Fahimeda Ali, Albert J. Allen, Albert J. Allen, Alysha K. Croker, Andrew J. Davidson, Pamela Dicks, Saul N. Faust, Saul N. Faust, Dionna Green, Collin Hovinga, Collin Hovinga, Agnes V. Klein, Robyn Langham, Hidefumi Nakamura, Laura Pioppo, Shiva Ramroop, Michiyo Sakiyama, Isabel Sanchez Vigil de la Villa, Junko Sato, Donna L. Snyder, Mark A. Turner, Mark A. Turner, Sarah Zaidi, Kanecia Zimmerman, Kanecia Zimmerman, Thierry Lacaze-Masmonteil

    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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    Indrukke van die XVIth Congress of the International Organisation for the Study of the Old Testament (IOSOT), Oslo, Noorweë by S D Snyman

    Published 1998-12-01
    “…Dit is waarskynlik die grootste Ou Testamentiese kongres ter wêreld met 'n bywoningtal van 400-500 mense vanuit Europa, Skandinawië, Amerika, Kanada, Brittanje, Japan, Israel, Australië en Afrika. …”
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