In medical device industry, the risk management is vital part of all your company’s processes, it involve in the entire lifecycle of a device. There are different risks raised from each process of a device marketed in China: market risk, regulatory risk and product quality risk. To ensure your company gets a safe and effective product to entry into Chinese market on time and reduce the regulatory risk, a successes implementation of risk assessment and management would be a best support for your business in China.
Please join in our “China Medical Device Regulatory Assistant Program” for free proposal. For complex and urgent projects, we will assign a dedicated project manager to customize a program specific to your requirements. We are ready to be of service at any time.
Contact Us
Mr. Edwin Wen China office
Tel: +86 571 8720 6541 | Fax: +86 571 8720 6533
Email: Edwin.wen@cirs-group.com
Mr. Michael Petersen China office
Tel: +86-571 8720 6559 | Fax: +86-571 8720 6533
Email: Elaine@cirs-group.com