Pharmaceuticals - , ,
Complya Asia provides expertise and guidance to help you meet your international cGMP compliance requirements. Working with your in-house experts, our Quality Assurance specialists will ensure your Quality Systems and facilities meet the current standards for US FDA, European EMA, and other international organizations.Complya Asia is a consulting company registered in China with headquarters in Suzhou (near Shanghai). We provide consulting services in the area of Quality Assurance and cGMP compliance. Our founders have an average of more than 20 years experience in pharmaceutical and medical device QA and cGMP operations. We have worked with numerous international and domestic companies throughout the US, Europe, and Asia who are developing therapeutic, vaccine, diagnostic and medical device products.智真生物医药技术咨询有限公司能提供专业技术和指导,帮助您达到国际cGMP符合性要求。我们的质量保证专员将和你们自身的专家一起工作,确保你们的质量体系和厂房设施满足美国FDA的现行标准,欧洲EMA和其他国际机构的标准。智真公司是一家在中国注册,总部位于苏州(临近上海)的咨询公司。我们提供质量保证领域和cGMP符合性领域的咨询服务。公司成立人在制药和医疗设施的QA和cGMP操作的平均从业经验均超过20年。我们和许多国内外的开发治疗、疫苗、诊断以及医疗设施产品的企业合作过,遍布了美国,欧洲和亚洲。