6 found
Order:
Disambiguations
Pamela Andanda [6]Pamela A. Andanda [1]
  1. Country Reports.Ma'N. H. Zawati, Don Chalmers, Sueli G. Dallari, Marina de Neiva Borba, Miriam Pinkesz, Yann Joly, Haidan Chen, Mette Hartlev, Liis Leitsalu, Sirpa Soini, Emmanuelle Rial-Sebbag, Nils Hoppe, Tina Garani-Papadatos, Panagiotis Vidalis, Krishna Ravi Srinivas, Gil Siegal, Stefania Negri, Ryoko Hatanaka, Maysa Al-Hussaini, Amal Al-Tabba', Lourdes Motta-Murgía, Laura Estela Torres Moran, Aart Hendriks, Obiajulu Nnamuchi, Rosario Isasi, Dorota Krekora-Zajac, Eman Sadoun, Calvin Ho, Pamela Andanda, Won Bok Lee, Pilar Nicolás, Titti Mattsson, Vladislava Talanova, Alexandre Dosch, Dominique Sprumont, Chien-Te Fan, Tzu-Hsun Hung, Jane Kaye, Andelka Phillips, Heather Gowans, Nisha Shah & James W. Hazel - 2019 - Journal of Law, Medicine and Ethics 47 (4):582-704.
    Direct download (3 more)  
     
    Export citation  
     
    Bookmark   1 citation  
  2.  12
    Regulation of Biobanks in South Africa.Pamela Andanda & Sandra Govender - 2015 - Journal of Law, Medicine and Ethics 43 (4):787-800.
    The ongoing efforts to establish biobanks in Africa envisage the availability of biological samples and data in accordance with relevant national legislation and ethical principles. Current literature has established that many African countries “do not have national legislation or guidelines on the use of stored biological samples” or if such guidelines are in place, then “disparities exist in relation to informed consent and export and import requirements.” In this regard, this article considers the extent to which the available legal and (...)
    No categories
    Direct download (6 more)  
     
    Export citation  
     
    Bookmark   3 citations  
  3.  39
    Module Two: Informed Consent.Pamela Andanda - 2005 - Developing World Bioethics 5 (1):14–29.
    ABSTRACTThe objective of this module is to familiarise you with the concept of informed consent, its ethical basis, its elements, and typical problems that are encountered even by the most well intentioned researchers when trying to achieve genuine informed consent.
    Direct download (4 more)  
     
    Export citation  
     
    Bookmark   5 citations  
  4.  9
    Human Dignity as a Basis for Providing Post-Trial Access to Healthcare for Research Participants: A South African Perspective.Pamela Andanda & Jane Wathuta - 2018 - Medicine, Health Care and Philosophy 21 (1):139-155.
    This paper discusses the need to focus on the dignity of human participants as a legal and ethical basis for providing post-trial access to healthcare. Debate about post-trial benefits has mostly focused on access to products or interventions proven to be effective in clinical trials. However, such access may be modelled on a broad fair benefits framework that emphasises both collateral benefits and interventional products of research, instead of prescribed post-trial access alone. The wording of the current version of the (...)
    Direct download (2 more)  
     
    Export citation  
     
    Bookmark   1 citation  
  5. The Law and Regulation of Clinical Research: Interplay with Public Policy and Bioethics.Pamela A. Andanda - 2006 - Focus Publilshers.
  6.  64
    Vulnerability: Sex Workers in Nairobi's Majengo Slum.Pamela Andanda - 2009 - Cambridge Quarterly of Healthcare Ethics 18 (2):138.
    Researchers from the Universities of Oxford, Nairobi, and Manitoba are collaborating on a project to develop an HIV vaccine based on the immunological protection mechanisms found in commercial sex workers from the Majengo slum in Nairobi. This group consists of educationally and economically disadvantaged women who resort to commercial sex work for a living. A clinic was established in the slum to study sexually transmitted diseases, which now includes HIV/AIDS. The clinic serves as a research facility for the collaborating researchers (...)
    Direct download (6 more)  
     
    Export citation  
     
    Bookmark