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. Shuo Wang (Head office)
Tel: +86-571 8720 6559 | Fax: +86-571 87206533
Email: md@cirs-group.com
Mr. Edwin Wen (Beijing office)
Tel: +86-10 63984062 | Fax: +86-10 63984032
Email: md@cirs-group.com

CIRS Europe

Bryan Zhou
Tel:  +353 (1)477 3710

Email: md@cirs-group.com

CIRS Korea
Mr. Junho Lee 
Tel: +82 2 6347 8801 
Email: md@cirs-group.com