Founded in 2016, Covar Pharmaceuticals specializes in guiding clients through the early development process, typically starting as early as pre-development through to conventional/hybrid Phase I and dose ranging Phase II studies. Covar possesses U.S. FDA, E.U. EMA, and Health Canada regulatory as well as U.S. FDA formulation development and CMC regulatory consulting capabilities. Covar also has an existing network of partners and capabilities in North America, including regulatory consulting for FDA matters and GMP analytical testing and early phase clinical supply manufacture capabilities in Mississauga, Canada. 科志康于2016年在张江药谷成立。基于法规政策、审评流程与决策机制,科志康建立了审评案例数据库,将新药研发咨询变为模块化和标准化,采用精细化的项目管理模式,替代了常规的专家咨询模式,既保障了服务品质,又大幅的降低了服务价格。 科志康咨询服务主要有三项,分别为非临床研究第三方项目管理、CMC法规咨询和志康论坛。科志康拥有超200家客户,超300个项目经验,中美IND获批超100个,NDA阶段项目19个,其中,有6个获NMPA批准,1个获FDA批准,另有8个ANDA获NMPA批准。 文章来源:科志康



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