Patient's Rights and the Practice of Obtaining Informed Consent: The Need for Some Corrective Measures
Jawaid, Shaukat Ali
Pakistan Journal of Medical Sciences 2006 January-March; 22(1); 7-9 [Online]. Accessed: http://pjms.com.pk/issues/janmar06/index.htm [2010 July 8]
Competence; Consent Forms; Consent; Developing Countries; Disclosure; Emergency Care; Ethics; Ethics Committees; Forms; Health; Health Literacy; Patients; Patients' Rights; Research; Research Ethics; Research Ethics Committees; Rights; Standards; Surgery; Third Party Consent; Informed Consent or Human Experimentation; Informed Consent;
Showing items related by title, author, creator and subject.
Wiseman, Oliver J.; Wijewardena, M.; Calleary, J.; Masood, J.; Hill, J.T. (2004-11)
Davis, Walter Alan; Holaday, John Graham (1994-03)
An act to amend the Human Rights Act of 1977 to prohibit employment discrimination based on genetic information; to prohibit an employer, employment agency, or labor organization from requesting or requiring a genetic test of, or administering a genetic test to, an employee or applicant for employment or membership; to prohibit an employer, employment agency, or labor organization from seeking to obtain, obtaining, or using genetic information of an employee or applicant for employment; to provide an exemption that allows the use of genetic testing or information with the written and informed consent of the employee or applicant for employment to determine the existence of a bona fide occupational qualification, investigate a workers' compensation or disability compensation claim, or determine an employee's susceptibility or exposure to potentially toxic substances in the workplace; to prohibit health benefit plans and health insurers from using genetic information as a condition of eligibility or in setting District of Columbia. Laws, statutes, etc. (2005-01-03)