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The in vitro diagnostic reagents registration measures for the administration of amendment (order no. 30 of the CFDA)
 
Author:中國銘鉉 企劃部  Release Time:2017-2-10 8:51:04  Number Browse:780
 

Administration of state food and drug supervision and administration

No. 30

The amendment to the in vitro diagnostic reagents registration measures for the administration on January 5, 2017, the state food and drug supervision and management of the administration, adopted at the meeting examined and approved, are hereby released, come into force from the date of release.

Chief: jingquan

On January 25, 2017

In vitro diagnostic reagents registration measures for the administration of the amendment

To paragraph 1 of article 20 is amended as: "article 17 and 18 of this regulation, mentioned in article 19 of the classification rules in vitro diagnostic reagent, used to guide the formulation and adjustment of the catalogs of in vitro diagnostic reagent, and determine the type of the new management of in vitro diagnostic reagents. The state food and drug supervision and administration bureau can vary according to the risk of the in vitro diagnostic reagent, adjustments to the classification rules."

This amendment come into force from the date of release.

 
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