它是中国唯一一家临床前CRO实验室，其研究数据被美国食品药物管理局(FDA)和欧洲药品管理局(emea)接受为重要规章备案文件的一部分。
It is the only preclinical CRO laboratory in China whose data have been accepted by both the FDA and EMEA as part of successful regulatory filings.
欧洲药品管理局公布了其计划给予公众获取信息的数据库的潜在副作用的人力和兽医药品。
The European Medicines Agency has published its plans for granting public access to the information held in its databases of the potential side effects of human and veterinary medicines.
欧洲药品管理局公布了其计划给予公众获取信息的数据库的潜在副作用的人力和兽医药品。
The European Medicines Agency has published its plans for granting public access to the information held in its databases of the potential side effects of human and veterinary medicines.
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