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In accordance with the "Administrative Measures for Post-Marketing Changes of Drugs (Trial)" (No.
We sincerely welcome valuable comments and suggestions from all walks of life on the solicitation draft, and timely feedback to us for follow-up improvement
Please send your feedback to the mailbox of the following contact:
Contact: Zhou Mengdie
Contact: jwba@cde.
Thank you for your participation and great support
Attachment: 1.
2.
3.
Drug Evaluation Center of the State Drug Administration
August 30, 2021
attachment1 : | Procedures and requirements for filing changes of overseas-produced drugs after marketing (draft for soliciting comments). |
Annex 2: | Drafting instructions. |
Annex 3 : | Feedback form. docx |
Attachment 1:
Procedures and requirements for filing changes of overseas-produced drugs after marketing (draft for comments ).
Annex 2:
Drafting instructions.
Annex 3:
Feedback form.
docx
Annex 1:
Procedures for filing changes of overseas-produced drugs after marketing And Requirements (Draft for Solicitation of Comments).
Attachment 1:
Procedures and requirements for filing changes to overseas-produced drugs after marketing (draft for comments).
pdf Procedures and requirements for filing changes to overseas-produced drugs after marketing (draft for comments).
Appendix 2:
Drafting Instructions.
Appendix 2:
Drafting Instructions.
pdf Drafting Instructions.
Appendix 3:
Feedback Form.
docx
Appendix 3:
Feedback Form.
docx Feedback Form.
docx