National post-market surveillance assessment of veterinary medicines in Korea during the past decade

Author:

Kang JeongWoo,Park Hae-chul,Jang Yang ho,Hossain Md Akil,Jeong Kyunghun,Jeong Mi young,Yun Seon-Jong,Park Sung-won,Kim Dae gyun,Lee Kwang-jickORCID

Funder

Animal and Plant Quarantine Agency

Publisher

Springer Science and Business Media LLC

Subject

General Veterinary,General Medicine

Reference16 articles.

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).

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