Table. 3.
Facility, personnel, and equipment criteria according to the Reimbursement Standard Notice
| Facility: Healthcare institutions that meet all of the following conditions: |
| a) Genetic testing institutions reported in accordance with Article 49 of the “Act on Bioethics and Safety” |
| b) Institutions that have received “Genetic Testing Accuracy Evaluation” three times or more in accordance with Article 48 of the “Enforcement Rules of the Act on Bioethics and Safety” |
| c) Institutions that meet all the conditions of (1)-(3) in the “Genetic Testing Accuracy Evaluation” of b) as of the date of healthcare coverage implementation: |
| (1) A-grade operation of the testing laboratory |
| (2) Results of on-site inspection in evaluation categories 1 and 3 are A-grade |
| (3) Scores of evaluation categories 1 and 3 in external proficiency testing are both average 90 points or higher |
| Personnel: Requires at least one full-time laboratory medicine or pathology specialists with more than five years of experience after obtaining specialist qualification, and at least one full-time clinical laboratory technicians. |
| Equipment: The resolution of testing equipment and Biochips (DNA Chips) should be 400 kb or higher. |
Lab Med Online 2023;13:141~153 https://doi.org/10.47429/lmo.2023.13.3.141
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