Tags: | NMPA | Pharmaceuticals | Drug | 药监局 | 医药品 | 药品 |
ITEM
COST
TIME
NOTE
China SFDA Registration consulting & Legal responsibility Agency
Contact us
1 Months
Technical documents Translation
0.5-1 Months
SDA registration Dossier Draft, Review and Submit
2-3 Months
NICPBP Pharmaceutical packaging materials Test & Follow up
4-6 Months
CDE Technical Evaluation Follow up Fee
6-9 Months
SFDA IPL Approval Follow up
3-4 Months
Other (Document Notarization etc.)
Total:
10-16
Months
Pre-Tax price