小春日和娜,早乙女壁纸

发布日期:2021年01月23日
Q & A – China NMPA (CFDA)
小春日和娜,早乙女壁纸

General Questions

General questions about China Regulatory Organization, NMPA (CFDA), CMDE.

Clinical Trials

Clinical Evaluation Report (CER), Clinical Trial and Overseas Clinical Data.

Registration

Registration, Renewal, Modification and Innovation Approval.

QMS/PMS

Quality Management System (QMS), Post Market Surveillance (PMS), Overseas Inspection.

小春日和娜,早乙女壁纸

Product Specific

Find product-specific questions and answers, sorted by the medical device/IVD/CDx product category.

Risk Evaluation

Answers about the risk assessment, in particular for the Periodic Risk Evaluation Report (PRER).