Complya Asia provides support for cGMP manufacturing and quality systems in Asia. We focus on helping our clients to achieve their goals of high quality manufacturing and meeting international standards for quality assurance.Registered in China with headquarters in Suzhou (near Shanghai), 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. Complya Asia provides expertise and guidance to help pharmaceutical, biotechnology and medical device companies meet international cGMP compliance requirements. Our founders have extensive experience in pharmaceutical and medical device QA and cGMP operations. Our sister company Complya Consulting Group LLC in Boston brings additional resources to our clients. 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, Chinese CFDA and other international organizations.
Contact: Juan Shao
Add: Address: 2F, Building 4, No. 99, Suqian Road, Suzhou, China, 215021