Solutions & Case Studies

Either the establishment in China or the foreign establishment that wants to enter China medical device market under CFDA regulations may encounter some unexpected issues, as well as some other problems involved with medical device regulations. CIRS’s medical devices department is a particularly professional team and has affluent experience in various medical devices; we are performing as your local regulatory staffs and aiming to provide practical and individual solutions for your products. In addition, the case studies those are conducted by our team are offered for your concern, which have obtained the agreement of releasing from our customers in advance.
 
Our solutions

  1. China Medical Device Regulatory Assistant Program (MDRAP)
  2. China Authorized Representative
  3. Case Studies
Contact Us
CIRS China

Ms. Elaine (Head office)
Tel: +86-571 87206559 | Fax: +86-571 87206533
Email: md@cirs-group.com
Mrs.Emily (Beijing office)
Tel: +86-10 63984062 | Fax: +86-10 63984032
Email: md@cirs-group.com

CIRS Europe

Ms. Louise Halpin
Tel: +353 41 9806 916 | Fax: +353 41 9806 999
Email: md@cirs-group.com