1. MAFRA. Handling rules of veterinary medicinal products. Notification No. 165.
http://www.law.go.kr/%EB%B2%95%EB%A0%B9/%EB%8F%99%EB%AC%BC%EC%9A%A9%EC%9D%98%EC%95%BD%ED%92%88%EB%93%B1%EC%B7%A8%EA%B8%89%EA%B7%9C%EC%B9%99/
(00165,20151005) (accessed 29 Jan 2017).
2. Kramer DB, Tan YT, Sato C, Kesselheim AS. Postmarket Surveillance of Medical Devices: A Comparison of Strategies in the US, EU, Japan, and China. PLoS Med. 2013;10(9):e1001519.
3. Lee KJ. GMP Guideline lecture of Veterinary drugs. MAFRA. 2013;37(3):120–4.
4. Jang HJ, Park SW, Yun SM, et al. Post-market surveillance assay of veterinary medicines in Korea. J Vet Publ Hlth. 2009;33(3):147–51.
5. MAFRA. Tip for inspecting a veterinary pharmaceutical affair. Directive No. 78.
http://www.law.go.kr/admRulLsInfoP.do?admRulSeq=2000000025687
(accessed 28 Jan 2017).