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1 Shin HY. Improving the Efficiency of IRB through Joint IRB in Multicenter Clinical Trials in Korea. Kor J Clin Pharmacol Ther, 2009;17(1):44-50. (Korean)/ View Article
2 이성희, 최병인, 김철민, 김경수. 의약품 임상시험 및 피험자 동의서에 대한 인식도. 대한임상약리학회지 17(1):72-92, 2009./ View Article
3 이성희, 최병인, 김철민, 김경수. 의약품 임상시험 및 피험자 동의서에 대한 인식도. 임상약리학회지 17(1):72-92, 2009./ View Article
4 심명진, 임영채. 임상연구 동의과정의 새로운 분류와 각 단계별 개선방안. 임상약리학회지 17(1):5-26, 2009./ View Article
5 Lee SH, Choi BI, Kim CM, Kim KS. A Survey on Perception of Clinical Trial of Pharmaceuticals and Informed Consent in Korea. Kor J Clin Pharmacol Ther 2009;17(1):72-92. (Korean)/ View Article
6 Shim MJ, Lim YC. Novel Classification of the Informed Consent Process in Clinical Research and the Ways to Improve Each Detailed Stage. Kor J Clin Pharmacol Ther. 2009;17(1):5-26. (Korean)/   DOI   Ndsl View Article
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