The safety evaluation of drugs refers to drugs non-clinical safety evaluation, or drugs non-clinical research, whose quality management practices are called Good Laboratory Practice (GLP).
药物安全性评价是指药物非临床安全评价即药物非临床研究，药物非临床研究质量管理规范即GLP。
This paper analyzed and expressed the relationship and difference between non-clinical trial and ADR monitoring, lead a comprehensive understanding of drug safety evaluation.
本文旨在通过对药品非临床研究与ADR监测区别与联系的分析，阐明二者之间的联系，使人们对药品安全性评价加以全面的认识。
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