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NL: Patients to get more control of their medical records

Posted on January 13, 2011 by Dissent

DutchNews.nl reports: Patients are to get the right to decide who should have access to their confidential medical details when they are stored in a central data bank, health minister Edith Schippers is set to announce on Thursday. The minister also wants patients to be automatically sent an email or mobile phone text message if…

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UK: Not breach of rights to force doctor to disclose patient records

Posted on January 13, 2011 by Dissent

Matt Donmall reports: A Swedish professor has failed in his European Court of Human Rights challenge to his conviction for disobeying a court order to hand over sensitive information in medical research, despite having promised the participants that the information would be for his use alone. As reported in a past blog, the fact of their…

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UK: NHS records viewed in India – SBS answers my questions

Posted on January 13, 2011 by Dissent

Tony Collins writes: NHS Shared Business Services – a joint venture between the Department of Health and Steria – does not have to publish any detail on what NHS information is viewed in India or what data fields can be viewed. Steria employs 5,000 in India some of whom work on NHS records. It says…

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GA: Lawmakers may monitor use of medications

Posted on January 13, 2011 by Dissent

Charles Oliver reports: The General Assembly may be taking a look in your medicine chest. Rep. Tom Weldon, R-Ringgold, said Thursday he will introduce legislation this year to battle “pill mills.” “We don’t have a searchable database that sheriffs and law enforcement can go in and see who has been buying meth products and who…

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Article: Relative Futility: Limits to Genetic Privacy Protection Because of the Inability to Prevent Disclosure of Genetic Information by Relatives

Posted on January 13, 2011 by Dissent

Relative Futility: Limits to Genetic Privacy Protection Because of the Inability to Prevent Disclosure of Genetic Information by Relatives Trevor Woodage Minnesota Law Review, December 2010, Volume 95, No. 2 Abstract: The Note considers possible limits to reasonable expectations of genetic privacy given that people share their DNA sequences with their relatives. Most scholars and…

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IE: Assessing the impact on privacy

Posted on January 10, 2011 by Dissent

Lloyd Mudiwa reports: Under the Health Act 2007, the Health Information and Quality Authority (HIQA) has the remit for setting standards for all aspects of health information and to monitor compliance with those standards. Prof Jane Grimson, Director of Health Information at HIQA, told Irish Medical Times that as part of this work, the Authority has…

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