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1)  Healthy subject
正常受试者
2)  subject [英]['sʌbdʒikt]  [美]['sʌbdʒɪkt]
受试者
1.
Study on Legal Protection of Subject s Right of Informed Consent in Clinical Trial;
对临床试验中“受试者知情同意权”法律保护的研究
2.
Moreover,we claim that for the purpose of scientific and reliable clinical research,the legal rights of subjects and the quality increase of ethics censorship,it is necessary to establish complete ethics censorship procedure and standard,intensify the training of the ethics committee s members,set up supervisory system and promote international comm.
对我国目前药物临床试验伦理审查存在的问题进行了分析,并提出通过建立完善的伦理审查程序和审查标准,加强伦理委员会成员的培训,加大国际间的交流及监管力度等措施,提高伦理审查的质量和水平,以保障受试者的合法权益和临床研究的科学性和可靠性。
3.
In view that clinical trial is different from traditional medical treatment procedure,the existing system is inadequate in protecting subjects safety and legal rights.
鉴于临床试验异于常规的特点,目前的体制不足以保护临床试验受试者的权益。
3)  subjects [英]['sʌbdʒikt]  [美]['sʌbdʒɪkt]
受试者
1.
According to valid law,injuries of subjects in clinical trials can only be judged by the principle of fault responsibility.
根据现行法律,临床试验中受试者受到损害只能适用过错责任归责原则。
4)  healthy donor
正常供者
1.
Peripheral blood hematopoietic stem cells mobilization with G-CSF in healthy donors;
粒细胞集落刺激因子动员正常供者外周血造血干细胞研究
5)  official receiver
正式收受者
6)  healthy volunteers
健康受试者
1.
Pharmacokinetic study of palonosetron in Chinese healthy volunteers;
我国健康受试者体内帕洛诺司琼的药物动力学研究
2.
OBJECTIVE To study the pharmacokinetics of cyclosporin A (CsA) with or without combination with berberine hydrochloride(Ber) in healthy volunteers.
目的 :研究健康受试者合用盐酸黄连素 (berberinehydrochloride ,Ber)前后环孢素A(cyclosporinA ,CsA)的动力学过程 ,以分析两药相互作用发生的部位。
补充资料:正常(超导)—超导(正常)转变
正常(超导)—超导(正常)转变

transitionfromnormal(superconducting)statetosuperconducting(normal)state

一般指在常压下改变温度到Tc时,物质的电阻从R>0(R=0)的正常态(超导态)到R=0(R>0)的超导态(正常态)的转变。无磁场时这种转变属二级相变。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。
参考词条