aportes a la gestión necesaria para la sustentabilidad de la SALUD PÚBLICA como figura esencial de los servicios sociales básicos para la sociedad humana, para la familia y para la persona como individuo que participa de la vida ciudadana.
sábado, 4 de marzo de 2017
PHG Foundation | Europe moves to prevent genetic discrimination and insurance
The Council of Europe has called on member states to strengthen the protection of health-related and genetic data held by insurance companies.
A newRecommendation has been adopted that seeks to protect the rights of people whose personal data are processed for insurance purposes . It is said to take into 'account insurance companies legitimate interest in assessing the level of risk presented by the insured person’ alongside safeguards for the collection and processing of relevant health-related personal data, based on the insured person’s consent. In particular, it is concerned with facilitating affordable access to health insurance for ’persons presenting an increased health risk’.
The Recommendation also proposes that genetic tests for the purposes of insurance (that is, obliging prospective customers to undergo predictive genetic tests) should be banned, although the UK is not obliged to enact the Council’s proposal. It requires justification of any use of family history or pre-existing genetic test results in calculating risk.
Most insurers in the UK currently operate under a voluntary moratorium agreed between the Association of British Insurers (ABI) and the government. This prohibits the use of data from genetic testing results for health or life insurance (with the exception of high-value policies and the dominantly inherited, very high penetrancecondition Huntingdon’s Disease) This was first agreed in 2001 and currently extending until 2019
Secretary General Jagland commented: “People’s health and genetic data are highly sensitive and must be properly protected. Governments have duty to ensure nobody is discriminated on the grounds of his or her genetic characteristics”.
Dr Mark Bale, chair of the Council of Europe’s Committee on Bioethics, which developed the new Recommendation, observed that: “What we wanted to try and do was to balance the human rights about personal data as well as the interests of the insurers”.
ver historia personal en: www.cerasale.com.ar [dado de baja por la Cancillería Argentina por temas políticos, propio de la censura que rige en nuestro medio]//
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