Hall R L
Toxicol Pathol. 1992;20(3 Pt 2):472-6. doi: 10.1177/0192623392020003202.
Regulatory guidelines for preclinical safety assessment studies of new drugs, chemicals, and food additives exist in many large industrial countries. Current guidelines include recommendations or requirements for clinical pathology testing. Many of the testing requirements are similar for every country, but others are not. The similarities and differences among several of the guidelines are discussed, and specific instances of ambiguous or inappropriate testing requirements are cited.
许多大型工业国家都存在针对新药、化学品和食品添加剂的临床前安全性评估研究的监管指南。现行指南包括临床病理学检测的建议或要求。每个国家的许多检测要求是相似的,但也有一些不同。本文讨论了其中几项指南之间的异同,并列举了模糊或不适当检测要求的具体实例。