要保持最新,他们持续地监测文学。 因此他们是一个被重视的信息资源为想要了解产品环境的商业作用在组织之内。[translate] aPreclinical Research and Clinical Trials Preclinical研究和临床试验[translate]
aThe company is a preclinical stage biopharmaceutical company with a limited operating history. Biopharmaceutical product development is a highly speculative undertaking and involves a substantial degree of risk. The company does not currently have any product candidates in clinical trials or approved for ...
In Canada, 16.1% of total R&D in 2001 was directed towards basicresearch;44.1% to clinical trials, 7.9% to improvement in manufacturing processes, 7.9%topreclinicalstudies, and 24% to drug regulation submissions, bioavailability studies and
待解决 悬赏分:1 - 离问题结束还有 Preclinical Research and Clinical Trials问题补充:匿名 2013-05-23 12:21:38 临床前研究和临床试验 匿名 2013-05-23 12:23:18 潜伏期的研究和临床试验 匿名 2013-05-23 12:24:58 Preclinical研究和临床试验 匿名 2013-05-23 12:26:38 临床前研究和临床试...
英文: THE PRECLINICAL PHARMACOLOGY STUDIES OF LOMEFLOXACIN中文: 新氟喹诺酮抗菌药洛美沙星的临床前药理学研究 英文: Study on the preclinical pharmacology of acetylkitasamycin中文: 乙酰吉他霉素临床前药理学研究 英文: Preclinical and Phase Ⅰ Clinical Trials of Salvicine中文: 沙尔威辛临床前试验及Ⅰ期临床...
Study:Several ADCs are being evaluated in preclinical efficacy trials. Study Design:Different animal models of autoimmune diseases have been chosen based on the various targets of the different ADCs, including rodents and non-human primates. The indications involved are psoriasis (pso), inflammatory bo...
The dipeptide boronic acid analogue PS-341 is a potent and selective proteasome inhibitor in clinical trials for a variety of tumor types. In vitro and in vivo (murine xenograft) studies show that PS-341 has activity against a variety of malignancies, including myeloma, chronic lymphocytic ...
is focusedonpreclinicalandclinical trials and improvement of manufacturing processes rather than onthedevelopmentofnew molecules.56 In both countries [...] iprcommission.org iprcommission.org 而在加拿大,研发活动却有大幅度的增加,部分是因为与跨国制药商达成的一项交易,而且 1987 年的所得税法案允许课税扣除...
aCharles River has the experience, range of services, and expertise to help you successfully initiate and complete critical phases of preclinical drug development by designing, performing, and documenting safety tests that meet the appropriate regulatory requirements before and after clinical trials begin...