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- About us
1. Regulatory Affairs Consulting
2. Drug Registration
To provide full-service for drug registration in China.
To provide full-service for API Filing in China.
4. Pharmaceutical Excipients Filing
To provide full-service for Pharmaceutical Excipients Filing in China.
5. Container Closure System Filing
To provide full-service for Container Closure System Filing in China.
7. Dossier Review
To review the technical documents to help the applicants prepare the dossier as required by China regulation.
8. Dossier Translation
To translate the dossier.
9. Dossier Preparation and Sorting
To prepare and sort the dossier as required by China regulation.
10. Dossier Submission
To submit the Registration Application to NMPA for acceptance.
11. Follow-up and Communication with NMPA
To follow up the review and approval as well as keep good communication with NMPA and applicants.
12. Legal Agent
To provide the applicant with the identity of the registration agency in China and to perform the relevant duties and obligations.
2. Professional and Experienced team The average working time in R & D and registration is 12 years.
3. High-quality Service High-quality and efficient services to assure promoting the marketization of products in China.