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05
2024
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12
ZJFDA(20160914) Notice of Zhejiang Food and Drug Administration on the Implementation of Registration Charges for Drugs and Medical Devices
ZJFDA（20160914) Notice of Zhejiang Food and Drug Administration on the Implementation of Registration Charges for Drugs and Medical Devices
Details: The document sets out the registration fees and payment procedures for drugs and medical device products.9Month15The day began to implement. The new API charges are as follows,
1.Supplementary application registration fee: change in the validity period of domestically produced drugs (6000Yuan), drug production enterprises within the change of drug production sites (31500Yuan), change the packaging materials or containers that directly contact the drug (31500Yuan);
2.Re-registration fee (once every five years) (29700Yuan);
3.The Measures for the Administration of Drug Registration belong to the Zhejiang Food and Drug Administration.
No registration fee for supplementary applications for drugs in the case will be charged. Belong
Zhejiang Food and Drug Administration approved the change of domestic drug production enterprises.
The registration fee is waived for supplementary applications for business names.
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