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Article
Affiliation(s)

University of Papua New Guinea, Waigani, PNG
University of Papua New Guinea, Taurama, PNG

ABSTRACT

The paper looks at how to regulate access to genetic testing, other than through a medical practitioner as part of health services provision. It examines the steps by which genetic testing services may be obtained from laboratories and the implications of these processes for individual access to testing services. It also discusses the quality assurance and accreditation standards which regulate genetic testing laboratories. Further, this paper looks into issues concerning the availability of home use testing or over-the-counter. Furthermore, we consider whether there should be additional legal protection against the taking and testing of genetic samples without the knowledge and consent of the individual concerned through the use of criminal sanctions.

KEYWORDS

genetic testing, medical practitioner, health services, legal protection, Papua New Guinea

Cite this paper

Psychology Research, March 2025, Vol. 15, No. 3, 118-124

References

urrow, B., Greaney, T., Johnson, S., Jost, T., & Schwartz, R. (2004). Bioethics: Health care law and ethics (5th ed.). St. Paul: West Publishing Company USA.

Minei, A. P., & Kaipu, S. O. (2020). Challenges of obtaining informed consent in poorly coordinated and funded healthcare services: Papua New Guinea situation. Journal of Health Science, 8, 135-152. doi:10.17265/2328-7136/2020.04.004

Minei, A. P., Arafia, R. A., & Roldan, R. R. (Jr). (Nov. 2018). Knowledge, awareness, and attitude of doctors and patients regarding informed consent to medical procedures in Papua New Guinea. Journal of Health Science, 6, 406-413. doi:10.17265/2328-7136/2018.06.002

Minei, A. P., Kaipu, S. O., & Minei, J. M. (2020). Culture within informed consent: Papua New Guinea perspective. Journal of Health Science, 8, 33-51. doi:10.17265/2328-7136/2020.02.001

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