On April 14, the General Department of the State Food and Drug Administration issued an announcement stating that in accordance with the requirements of the "Administrative Measures for Medical Device Standards" and "Administrative Specifications for the Formulation and Revision of Medical Device Standards", the State Food and Drug Administration organized and carried out the revision of the medical device industry standards in 2022.
In the project selection work, after public consultation and expert demonstration, 116 medical device industry standard formulation and revision plan projects in 2022 have been determined, which are hereby announced
.
During the publicity period, if you have any objection, please report it to the State Food and Drug Administration
.
Announcement time: 7 days from the date of the announcement by the State Food and Drug Administration E-mail: mdct@nmpa.
gov.
cn (please specify "2022 Industry Standard Revision Project Feedback" in the subject of the email) Attachment: 1.
2022 Medical Device Mandatory Sex industry standard formulation and revision plan project 2.
2022 medical device recommended industry standard formulation and revision plan project
In the project selection work, after public consultation and expert demonstration, 116 medical device industry standard formulation and revision plan projects in 2022 have been determined, which are hereby announced
.
During the publicity period, if you have any objection, please report it to the State Food and Drug Administration
.
Announcement time: 7 days from the date of the announcement by the State Food and Drug Administration E-mail: mdct@nmpa.
gov.
cn (please specify "2022 Industry Standard Revision Project Feedback" in the subject of the email) Attachment: 1.
2022 Medical Device Mandatory Sex industry standard formulation and revision plan project 2.
2022 medical device recommended industry standard formulation and revision plan project
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