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On December 1, the Comprehensive Department of the State Food and Drug Administration issued an announcement stating that, in order to implement the Pharmaceutical Administration Law of the People’s Republic of China and the Vaccine Administration Law of the People’s Republic of The Bureau organized the drafting of the "Guiding Principles for Pharmacovigilance Inspection (Draft for Soliciting Comments)" (see Annex 1), which is now open to the public for comments
Please fill in the feedback form (see Annex 2) and send it to the email address: sunyang@nmpa.
Appendix:
1.
Guidelines for Pharmacovigilance Inspection (Draft for Solicitation of Comments)
2.
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